Lower thoracic kyphosis [hp:0004633]
type: SIO_010056
comment: Phenotype [hp:0004633] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lower thoracic kyphosis
in dataset: phenotype

Congenital neutropenia [hp:0005549]
type: SIO_010056
comment: Phenotype [hp:0005549] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital neutropenia
in dataset: phenotype

Congenital finger flexion contractures [hp:0005879]
type: SIO_010056
comment: Phenotype [hp:0005879] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital finger flexion contractures
in dataset: phenotype

Purpura [hp:0000979]
type: SIO_010056
comment: Phenotype [hp:0000979] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Purpura
in dataset: phenotype

Paralysis [hp:0003470]
type: SIO_010056
comment: Phenotype [hp:0003470] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paralysis
in dataset: phenotype

Type 1 muscle fiber predominance [hp:0003803]
type: SIO_010056
comment: Phenotype [hp:0003803] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type 1 muscle fiber predominance
in dataset: phenotype

Irregular proximal tibial epiphyses [hp:0006456]
type: SIO_010056
comment: Phenotype [hp:0006456] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular proximal tibial epiphyses
in dataset: phenotype

Chorioretinal dysplasia [hp:0007731]
type: SIO_010056
comment: Phenotype [hp:0007731] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chorioretinal dysplasia
in dataset: phenotype

Hypoplastic right heart [hp:0010954]
type: SIO_010056
comment: Phenotype [hp:0010954] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic right heart
in dataset: phenotype

Fused cervical vertebrae [hp:0002949]
type: SIO_010056
comment: Phenotype [hp:0002949] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fused cervical vertebrae
in dataset: phenotype

Premature fusion of phalangeal epiphyses [hp:0006140]
type: SIO_010056
comment: Phenotype [hp:0006140] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature fusion of phalangeal epiphyses
in dataset: phenotype

Abnormal natural killer cell physiology [hp:0012177]
type: SIO_010056
comment: Phenotype [hp:0012177] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal natural killer cell physiology
in dataset: phenotype

Limb joint contracture [hp:0003121]
type: SIO_010056
comment: Phenotype [hp:0003121] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb joint contracture
in dataset: phenotype

Agammaglobulinemia [hp:0004432]
type: SIO_010056
comment: Phenotype [hp:0004432] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Agammaglobulinemia
in dataset: phenotype

Chronic CSF lymphocytosis [hp:0009704]
type: SIO_010056
comment: Phenotype [hp:0009704] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic CSF lymphocytosis
in dataset: phenotype

Osteolysis [hp:0002797]
type: SIO_010056
comment: Phenotype [hp:0002797] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteolysis
in dataset: phenotype

Abnormality of the aorta [hp:0001679]
type: SIO_010056
comment: Phenotype [hp:0001679] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the aorta
in dataset: phenotype

Abolished electroretinogram (ERG) [hp:0000550]
type: SIO_010056
comment: Phenotype [hp:0000550] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abolished electroretinogram (ERG)
in dataset: phenotype

Abnormality of the tonsils [hp:0100765]
type: SIO_010056
comment: Phenotype [hp:0100765] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the tonsils
in dataset: phenotype

Foot dorsiflexor weakness [hp:0009027]
type: SIO_010056
comment: Phenotype [hp:0009027] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Foot dorsiflexor weakness
in dataset: phenotype

Blurred vision [hp:0000622]
type: SIO_010056
comment: Phenotype [hp:0000622] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Blurred vision
in dataset: phenotype

Recurrent Aspergillus infections [hp:0002724]
type: SIO_010056
comment: Phenotype [hp:0002724] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent Aspergillus infections
in dataset: phenotype

Gastric ulcer [hp:0002592]
type: SIO_010056
comment: Phenotype [hp:0002592] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gastric ulcer
in dataset: phenotype

Pituitary growth hormone cell adenoma [hp:0011760]
type: SIO_010056
comment: Phenotype [hp:0011760] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pituitary growth hormone cell adenoma
in dataset: phenotype

Ectopic ossification [hp:0011986]
type: SIO_010056
comment: Phenotype [hp:0011986] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopic ossification
in dataset: phenotype

Abnormality of the philtrum [hp:0000288]
type: SIO_010056
comment: Phenotype [hp:0000288] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the philtrum
in dataset: phenotype

Corticospinal tract hypoplasia [hp:0007016]
type: SIO_010056
comment: Phenotype [hp:0007016] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corticospinal tract hypoplasia
in dataset: phenotype

Biceps aplasia [hp:0009783]
type: SIO_010056
comment: Phenotype [hp:0009783] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Biceps aplasia
in dataset: phenotype

Bruising susceptibility [hp:0000978]
type: SIO_010056
comment: Phenotype [hp:0000978] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bruising susceptibility
in dataset: phenotype

Glutaric acidemia [hp:0003530]
type: SIO_010056
comment: Phenotype [hp:0003530] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glutaric acidemia
in dataset: phenotype

Megakaryocytopenia [hp:0005548]
type: SIO_010056
comment: Phenotype [hp:0005548] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Megakaryocytopenia
in dataset: phenotype

Cheekbone underdevelopment [hp:0010669]
type: SIO_010056
comment: Phenotype [hp:0010669] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cheekbone underdevelopment
in dataset: phenotype

Lower thoracic interpediculate narrowness [hp:0008470]
type: SIO_010056
comment: Phenotype [hp:0008470] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lower thoracic interpediculate narrowness
in dataset: phenotype

Cuboid-shaped vertebral bodies [hp:0004634]
type: SIO_010056
comment: Phenotype [hp:0004634] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cuboid-shaped vertebral bodies
in dataset: phenotype

Clinodactyly of the 5th finger [hp:0004209]
type: SIO_010056
comment: Phenotype [hp:0004209] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Clinodactyly of the 5th finger
in dataset: phenotype

Lester's sign [hp:0009781]
type: SIO_010056
comment: Phenotype [hp:0009781] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lester's sign
in dataset: phenotype

Iris hypopigmentation [hp:0007730]
type: SIO_010056
comment: Phenotype [hp:0007730] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Iris hypopigmentation
in dataset: phenotype

Arterial thrombosis [hp:0004420]
type: SIO_010056
comment: Phenotype [hp:0004420] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arterial thrombosis
in dataset: phenotype

Systemic lupus erythematosus [hp:0002725]
type: SIO_010056
comment: Phenotype [hp:0002725] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Systemic lupus erythematosus
in dataset: phenotype

Loss of consciousness [hp:0007185]
type: SIO_010056
comment: Phenotype [hp:0007185] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Loss of consciousness
in dataset: phenotype

Impairment of fructose metabolism [hp:0011033]
type: SIO_010056
comment: Phenotype [hp:0011033] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impairment of fructose metabolism
in dataset: phenotype

Increased hepatic glycogen content [hp:0006568]
type: SIO_010056
comment: Phenotype [hp:0006568] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased hepatic glycogen content
in dataset: phenotype

Ebstein's anomaly of the tricuspid valve [hp:0010316]
type: SIO_010056
comment: Phenotype [hp:0010316] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ebstein's anomaly of the tricuspid valve
in dataset: phenotype

Complement deficiency [hp:0004431]
type: SIO_010056
comment: Phenotype [hp:0004431] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Complement deficiency
in dataset: phenotype

Vertebral fusion [hp:0002948]
type: SIO_010056
comment: Phenotype [hp:0002948] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vertebral fusion
in dataset: phenotype

Graves disease [hp:0100647]
type: SIO_010056
comment: Phenotype [hp:0100647] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Graves disease
in dataset: phenotype

Reduced natural killer cell activity [hp:0012178]
type: SIO_010056
comment: Phenotype [hp:0012178] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced natural killer cell activity
in dataset: phenotype

Lymphangioma [hp:0100764]
type: SIO_010056
comment: Phenotype [hp:0100764] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lymphangioma
in dataset: phenotype

Abnormality of color vision [hp:0000551]
type: SIO_010056
comment: Phenotype [hp:0000551] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of color vision
in dataset: phenotype

Ph-positive acute lymphoblastic leukemia [hp:0004848]
type: SIO_010056
comment: Phenotype [hp:0004848] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ph-positive acute lymphoblastic leukemia
in dataset: phenotype

Acholic stools [hp:0011985]
type: SIO_010056
comment: Phenotype [hp:0011985] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acholic stools
in dataset: phenotype

Entropion [hp:0000621]
type: SIO_010056
comment: Phenotype [hp:0000621] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Entropion
in dataset: phenotype

Intestinal lymphangiectasia [hp:0002593]
type: SIO_010056
comment: Phenotype [hp:0002593] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intestinal lymphangiectasia
in dataset: phenotype

Increased facial adipose tissue [hp:0000287]
type: SIO_010056
comment: Phenotype [hp:0000287] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased facial adipose tissue
in dataset: phenotype

Poor gross motor coordination [hp:0007015]
type: SIO_010056
comment: Phenotype [hp:0007015] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poor gross motor coordination
in dataset: phenotype

Vitamin B6 deficiency [hp:0008326]
type: SIO_010056
comment: Phenotype [hp:0008326] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vitamin B6 deficiency
in dataset: phenotype

Delayed proximal femoral epiphyseal ossification [hp:0008828]
type: SIO_010056
comment: Phenotype [hp:0008828] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed proximal femoral epiphyseal ossification
in dataset: phenotype

Deeply set eye [hp:0000490]
type: SIO_010056
comment: Phenotype [hp:0000490] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deeply set eye
in dataset: phenotype

Abnormal metaphyseal trabeculation [hp:0005089]
type: SIO_010056
comment: Phenotype [hp:0005089] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal metaphyseal trabeculation
in dataset: phenotype

Cutaneous leiomyoma [hp:0007620]
type: SIO_010056
comment: Phenotype [hp:0007620] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cutaneous leiomyoma
in dataset: phenotype

Cervical vertebrae fusion (C5/C6) [hp:0004635]
type: SIO_010056
comment: Phenotype [hp:0004635] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cervical vertebrae fusion (C5/C6)
in dataset: phenotype

Rimmed vacuoles [hp:0003805]
type: SIO_010056
comment: Phenotype [hp:0003805] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rimmed vacuoles
in dataset: phenotype

Progressive calcification of costochondral cartilage [hp:0006600]
type: SIO_010056
comment: Phenotype [hp:0006600] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive calcification of costochondral cartilage
in dataset: phenotype

C8 deficiency [hp:0004434]
type: SIO_010056
comment: Phenotype [hp:0004434] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: C8 deficiency
in dataset: phenotype

Diffuse demyelination of the cerebral white matter [hp:0007162]
type: SIO_010056
comment: Phenotype [hp:0007162] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse demyelination of the cerebral white matter
in dataset: phenotype

Soft skin [hp:0000977]
type: SIO_010056
comment: Phenotype [hp:0000977] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Soft skin
in dataset: phenotype

Resistance to activated protein C [hp:0012175]
type: SIO_010056
comment: Phenotype [hp:0012175] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Resistance to activated protein C
in dataset: phenotype

Duplication of the proximal phalanx of the hallux [hp:0010093]
type: SIO_010056
comment: Phenotype [hp:0010093] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Duplication of the proximal phalanx of the hallux
in dataset: phenotype

Attenuation of retinal blood vessels [hp:0007843]
type: SIO_010056
comment: Phenotype [hp:0007843] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Attenuation of retinal blood vessels
in dataset: phenotype

Hypomimic face [hp:0000338]
type: SIO_010056
comment: Phenotype [hp:0000338] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypomimic face
in dataset: phenotype

Laterally curved eyebrow [hp:0007733]
type: SIO_010056
comment: Phenotype [hp:0007733] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laterally curved eyebrow
in dataset: phenotype

Lissencephaly [hp:0001339]
type: SIO_010056
comment: Phenotype [hp:0001339] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lissencephaly
in dataset: phenotype

Elevated systolic blood pressure [hp:0004421]
type: SIO_010056
comment: Phenotype [hp:0004421] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated systolic blood pressure
in dataset: phenotype

Epicanthus [hp:0000286]
type: SIO_010056
comment: Phenotype [hp:0000286] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Epicanthus
in dataset: phenotype

Atretic gallbladder [hp:0011984]
type: SIO_010056
comment: Phenotype [hp:0011984] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atretic gallbladder
in dataset: phenotype

Attention deficit hyperactivity disorder [hp:0007018]
type: SIO_010056
comment: Phenotype [hp:0007018] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Attention deficit hyperactivity disorder
in dataset: phenotype

Breast hypertrophy [hp:0010313]
type: SIO_010056
comment: Phenotype [hp:0010313] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Breast hypertrophy
in dataset: phenotype

Hepatic encephalopathy [hp:0002480]
type: SIO_010056
comment: Phenotype [hp:0002480] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatic encephalopathy
in dataset: phenotype

Recurrent abscess formation [hp:0002722]
type: SIO_010056
comment: Phenotype [hp:0002722] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent abscess formation
in dataset: phenotype

Pancreatic hypoplasia [hp:0002594]
type: SIO_010056
comment: Phenotype [hp:0002594] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pancreatic hypoplasia
in dataset: phenotype

Abnormal finger flexion creases [hp:0006143]
type: SIO_010056
comment: Phenotype [hp:0006143] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal finger flexion creases
in dataset: phenotype

Spinal cord tumor [hp:0010302]
type: SIO_010056
comment: Phenotype [hp:0010302] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinal cord tumor
in dataset: phenotype

Functional respiratory abnormality [hp:0002795]
type: SIO_010056
comment: Phenotype [hp:0002795] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Functional respiratory abnormality
in dataset: phenotype

Carpal synostosis [hp:0009702]
type: SIO_010056
comment: Phenotype [hp:0009702] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Carpal synostosis
in dataset: phenotype

Absent/shortened outer dynein arms [hp:0200109]
type: SIO_010056
comment: Phenotype [hp:0200109] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent/shortened outer dynein arms
in dataset: phenotype

Coronary artery disease [hp:0001677]
type: SIO_010056
comment: Phenotype [hp:0001677] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coronary artery disease
in dataset: phenotype

Equinus calcaneus [hp:0008138]
type: SIO_010056
comment: Phenotype [hp:0008138] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Equinus calcaneus
in dataset: phenotype

Delayed femoral head ossification [hp:0008829]
type: SIO_010056
comment: Phenotype [hp:0008829] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed femoral head ossification
in dataset: phenotype

Restricted large joint movement [hp:0005193]
type: SIO_010056
comment: Phenotype [hp:0005193] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Restricted large joint movement
in dataset: phenotype

Triceps aplasia [hp:0009785]
type: SIO_010056
comment: Phenotype [hp:0009785] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triceps aplasia
in dataset: phenotype

Renal calcium wasting [hp:0012637]
type: SIO_010056
comment: Phenotype [hp:0012637] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal calcium wasting
in dataset: phenotype

Dupuytren contracture [hp:0005679]
type: SIO_010056
comment: Phenotype [hp:0005679] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dupuytren contracture
in dataset: phenotype

Abnormality of iron homeostasis [hp:0011031]
type: SIO_010056
comment: Phenotype [hp:0011031] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of iron homeostasis
in dataset: phenotype

Cherry red spot of the macula [hp:0010729]
type: SIO_010056
comment: Phenotype [hp:0010729] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cherry red spot of the macula
in dataset: phenotype

Lacrimal gland hypoplasia [hp:0007732]
type: SIO_010056
comment: Phenotype [hp:0007732] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lacrimal gland hypoplasia
in dataset: phenotype

Biparietal narrowing [hp:0004422]
type: SIO_010056
comment: Phenotype [hp:0004422] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Biparietal narrowing
in dataset: phenotype

Prominent protruding coccyx [hp:0008472]
type: SIO_010056
comment: Phenotype [hp:0008472] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent protruding coccyx
in dataset: phenotype

Abnormality of natural killer cells [hp:0012176]
type: SIO_010056
comment: Phenotype [hp:0012176] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of natural killer cells
in dataset: phenotype

Secretory IgA deficiency [hp:0004433]
type: SIO_010056
comment: Phenotype [hp:0004433] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Secretory IgA deficiency
in dataset: phenotype

Eczematoid dermatitis [hp:0000976]
type: SIO_010056
comment: Phenotype [hp:0000976] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Eczematoid dermatitis
in dataset: phenotype

Cone-shaped epiphysis of the 1st metacarpal [hp:0010017]
type: SIO_010056
comment: Phenotype [hp:0010017] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cone-shaped epiphysis of the 1st metacarpal
in dataset: phenotype

Neoplasm of the oral cavity [hp:0100649]
type: SIO_010056
comment: Phenotype [hp:0100649] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the oral cavity
in dataset: phenotype

Pugilistic facies [hp:0000339]
type: SIO_010056
comment: Phenotype [hp:0000339] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pugilistic facies
in dataset: phenotype

Focal T2 hyperintense basal ganglia lesion [hp:0007183]
type: SIO_010056
comment: Phenotype [hp:0007183] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Focal T2 hyperintense basal ganglia lesion
in dataset: phenotype

Ileus [hp:0002595]
type: SIO_010056
comment: Phenotype [hp:0002595] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ileus
in dataset: phenotype

Premature thelarche [hp:0010314]
type: SIO_010056
comment: Phenotype [hp:0010314] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature thelarche
in dataset: phenotype

Abnormality of oral mucosa [hp:0011830]
type: SIO_010056
comment: Phenotype [hp:0011830] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of oral mucosa
in dataset: phenotype

Absence of bactericidal oxidative 'respiratory burst' in phagocytes [hp:0002723]
type: SIO_010056
comment: Phenotype [hp:0002723] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of bactericidal oxidative 'respiratory burst' in phagocytes
in dataset: phenotype

Supranuclear ophthalmoplegia [hp:0000623]
type: SIO_010056
comment: Phenotype [hp:0000623] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Supranuclear ophthalmoplegia
in dataset: phenotype

Partial agenesis of the corpus callosum [hp:0001338]
type: SIO_010056
comment: Phenotype [hp:0001338] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Partial agenesis of the corpus callosum
in dataset: phenotype

Atrioventricular block [hp:0001678]
type: SIO_010056
comment: Phenotype [hp:0001678] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atrioventricular block
in dataset: phenotype

Aplasia/Hypoplasia of the pancreas [hp:0100800]
type: SIO_010056
comment: Phenotype [hp:0100800] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the pancreas
in dataset: phenotype

Spinal dysraphism [hp:0010301]
type: SIO_010056
comment: Phenotype [hp:0010301] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinal dysraphism
in dataset: phenotype

Flattened metatarsal heads [hp:0005194]
type: SIO_010056
comment: Phenotype [hp:0005194] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flattened metatarsal heads
in dataset: phenotype

Narrow anterio-posterior vertebral body diameter [hp:0008473]
type: SIO_010056
comment: Phenotype [hp:0008473] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow anterio-posterior vertebral body diameter
in dataset: phenotype

Progressive forgetfulness [hp:0007017]
type: SIO_010056
comment: Phenotype [hp:0007017] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive forgetfulness
in dataset: phenotype

Retinal vein occlusion [hp:0012636]
type: SIO_010056
comment: Phenotype [hp:0012636] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal vein occlusion
in dataset: phenotype

Hernia of the abdominal wall [hp:0004299]
type: SIO_010056
comment: Phenotype [hp:0004299] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hernia of the abdominal wall
in dataset: phenotype

Chronic mucocutaneous candidiasis [hp:0002728]
type: SIO_010056
comment: Phenotype [hp:0002728] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic mucocutaneous candidiasis
in dataset: phenotype

3-Methylglutaconic aciduria [hp:0003535]
type: SIO_010056
comment: Phenotype [hp:0003535] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 3-Methylglutaconic aciduria
in dataset: phenotype

Thin upper lip vermilion [hp:0000219]
type: SIO_010056
comment: Phenotype [hp:0000219] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thin upper lip vermilion
in dataset: phenotype

Orthostatic tachycardia [hp:0012173]
type: SIO_010056
comment: Phenotype [hp:0012173] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Orthostatic tachycardia
in dataset: phenotype

Amyloid deposition in the vitreous humor [hp:0007841]
type: SIO_010056
comment: Phenotype [hp:0007841] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Amyloid deposition in the vitreous humor
in dataset: phenotype

Reduced factor VIII activity [hp:0003125]
type: SIO_010056
comment: Phenotype [hp:0003125] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced factor VIII activity
in dataset: phenotype

High-frequency hearing impairment [hp:0005101]
type: SIO_010056
comment: Phenotype [hp:0005101] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High-frequency hearing impairment
in dataset: phenotype

Biconcave flattened vertebrae [hp:0003321]
type: SIO_010056
comment: Phenotype [hp:0003321] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Biconcave flattened vertebrae
in dataset: phenotype

Short 5th finger [hp:0009237]
type: SIO_010056
comment: Phenotype [hp:0009237] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short 5th finger
in dataset: phenotype

Abnormality of adipose tissue [hp:0009124]
type: SIO_010056
comment: Phenotype [hp:0009124] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of adipose tissue
in dataset: phenotype

Myotonia [hp:0002486]
type: SIO_010056
comment: Phenotype [hp:0002486] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myotonia
in dataset: phenotype

Abnormal pattern of respiration [hp:0002793]
type: SIO_010056
comment: Phenotype [hp:0002793] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal pattern of respiration
in dataset: phenotype

Periventricular gray matter heterotopia [hp:0007165]
type: SIO_010056
comment: Phenotype [hp:0007165] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Periventricular gray matter heterotopia
in dataset: phenotype

Hyperplastic callus formation [hp:0030268]
type: SIO_010056
comment: Phenotype [hp:0030268] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperplastic callus formation
in dataset: phenotype

Abnormally low-pitched voice [hp:0010300]
type: SIO_010056
comment: Phenotype [hp:0010300] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormally low-pitched voice
in dataset: phenotype

Somatic mosaicism [hp:0001442]
type: SIO_010056
comment: Phenotype [hp:0001442] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Somatic mosaicism
in dataset: phenotype

Uveitis [hp:0000554]
type: SIO_010056
comment: Phenotype [hp:0000554] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Uveitis
in dataset: phenotype

Visceral angiomatosis [hp:0100761]
type: SIO_010056
comment: Phenotype [hp:0100761] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Visceral angiomatosis
in dataset: phenotype

Oligohydramnios [hp:0001562]
type: SIO_010056
comment: Phenotype [hp:0001562] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oligohydramnios
in dataset: phenotype

Tremor [hp:0001337]
type: SIO_010056
comment: Phenotype [hp:0001337] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tremor
in dataset: phenotype

Aplasia/Hypoplasia of the breasts [hp:0010311]
type: SIO_010056
comment: Phenotype [hp:0010311] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the breasts
in dataset: phenotype

Abdominal wall muscle weakness [hp:0009023]
type: SIO_010056
comment: Phenotype [hp:0009023] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abdominal wall muscle weakness
in dataset: phenotype

Enlarged lacrimal glands [hp:0007734]
type: SIO_010056
comment: Phenotype [hp:0007734] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged lacrimal glands
in dataset: phenotype

Follicular hyperplasia [hp:0002729]
type: SIO_010056
comment: Phenotype [hp:0002729] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Follicular hyperplasia
in dataset: phenotype

Reduced xanthine dehydrogenase activity [hp:0003534]
type: SIO_010056
comment: Phenotype [hp:0003534] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced xanthine dehydrogenase activity
in dataset: phenotype

Anterior beaking of thoracic vertebrae [hp:0004630]
type: SIO_010056
comment: Phenotype [hp:0004630] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior beaking of thoracic vertebrae
in dataset: phenotype

Coombs-positive hemolytic anemia [hp:0004844]
type: SIO_010056
comment: Phenotype [hp:0004844] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coombs-positive hemolytic anemia
in dataset: phenotype

Agenesis of mandibular central incisor [hp:0006355]
type: SIO_010056
comment: Phenotype [hp:0006355] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Agenesis of mandibular central incisor
in dataset: phenotype

Hypercholesterolemia [hp:0003124]
type: SIO_010056
comment: Phenotype [hp:0003124] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypercholesterolemia
in dataset: phenotype

Glioblastoma multiforme [hp:0012174]
type: SIO_010056
comment: Phenotype [hp:0012174] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glioblastoma multiforme
in dataset: phenotype

Increased serum insulin-like growth factor 1 {comment="HPO:probinson"} [hp:0030269]
type: SIO_010056
comment: Phenotype [hp:0030269] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased serum insulin-like growth factor 1 {comment="HPO:probinson"}
in dataset: phenotype

Transient hypophosphatemia [hp:0008285]
type: SIO_010056
comment: Phenotype [hp:0008285] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Transient hypophosphatemia
in dataset: phenotype

Progressive flexion contractures [hp:0005876]
type: SIO_010056
comment: Phenotype [hp:0005876] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive flexion contractures
in dataset: phenotype

Premature birth following premature rupture of fetal membranes [hp:0005100]
type: SIO_010056
comment: Phenotype [hp:0005100] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature birth following premature rupture of fetal membranes
in dataset: phenotype

C1-C2 subluxation [hp:0003320]
type: SIO_010056
comment: Phenotype [hp:0003320] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: C1-C2 subluxation
in dataset: phenotype

Reduced vital capacity [hp:0002792]
type: SIO_010056
comment: Phenotype [hp:0002792] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced vital capacity
in dataset: phenotype

Lipodystrophy [hp:0009125]
type: SIO_010056
comment: Phenotype [hp:0009125] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lipodystrophy
in dataset: phenotype

Pigment gallstones [hp:0011981]
type: SIO_010056
comment: Phenotype [hp:0011981] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pigment gallstones
in dataset: phenotype

Palpitations (with pheochromocytoma) [hp:0001676]
type: SIO_010056
comment: Phenotype [hp:0001676] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palpitations (with pheochromocytoma)
in dataset: phenotype

Myoclonus [hp:0001336]
type: SIO_010056
comment: Phenotype [hp:0001336] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myoclonus
in dataset: phenotype

Shortening of all proximal phalanges of the fingers [hp:0006144]
type: SIO_010056
comment: Phenotype [hp:0006144] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shortening of all proximal phalanges of the fingers
in dataset: phenotype

Increased CSF interferon alpha [hp:0009709]
type: SIO_010056
comment: Phenotype [hp:0009709] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased CSF interferon alpha
in dataset: phenotype

Fetal polyuria [hp:0001563]
type: SIO_010056
comment: Phenotype [hp:0001563] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fetal polyuria
in dataset: phenotype

Clubbing of toes [hp:0100760]
type: SIO_010056
comment: Phenotype [hp:0100760] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Clubbing of toes
in dataset: phenotype

Leukocoria [hp:0000555]
type: SIO_010056
comment: Phenotype [hp:0000555] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Leukocoria
in dataset: phenotype

Acute monocytic leukemia [hp:0004845]
type: SIO_010056
comment: Phenotype [hp:0004845] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute monocytic leukemia
in dataset: phenotype

Severe combined immunodeficiency [hp:0004430]
type: SIO_010056
comment: Phenotype [hp:0004430] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe combined immunodeficiency
in dataset: phenotype

Abnormality of neuronal migration [hp:0002269]
type: SIO_010056
comment: Phenotype [hp:0002269] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of neuronal migration
in dataset: phenotype

Xerostomia [hp:0000217]
type: SIO_010056
comment: Phenotype [hp:0000217] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Xerostomia
in dataset: phenotype

Urinary bladder sphincter dysfunction [hp:0002839]
type: SIO_010056
comment: Phenotype [hp:0002839] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urinary bladder sphincter dysfunction
in dataset: phenotype

Bony spicule pigmentary retinopathy [hp:0007737]
type: SIO_010056
comment: Phenotype [hp:0007737] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bony spicule pigmentary retinopathy
in dataset: phenotype

Absent fifth toenail [hp:0200105]
type: SIO_010056
comment: Phenotype [hp:0200105] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent fifth toenail
in dataset: phenotype

Delayed oxidation of acetaldehyde [hp:0003533]
type: SIO_010056
comment: Phenotype [hp:0003533] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed oxidation of acetaldehyde
in dataset: phenotype

Amyloidosis [hp:0011034]
type: SIO_010056
comment: Phenotype [hp:0011034] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Amyloidosis
in dataset: phenotype

Partial duplication of the distal phalanx of the hallux [hp:0010097]
type: SIO_010056
comment: Phenotype [hp:0010097] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Partial duplication of the distal phalanx of the hallux
in dataset: phenotype

Recurrent Staphylococcus aureus infections [hp:0002726]
type: SIO_010056
comment: Phenotype [hp:0002726] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent Staphylococcus aureus infections
in dataset: phenotype

Camptodactyly [hp:0012385]
type: SIO_010056
comment: Phenotype [hp:0012385] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Camptodactyly
in dataset: phenotype

Delayed patellar ossification [hp:0006454]
type: SIO_010056
comment: Phenotype [hp:0006454] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed patellar ossification
in dataset: phenotype

Calcification of the auricular cartilage [hp:0005103]
type: SIO_010056
comment: Phenotype [hp:0005103] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcification of the auricular cartilage
in dataset: phenotype

Asymmetry of intraocular pressure [hp:0012633]
type: SIO_010056
comment: Phenotype [hp:0012633] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Asymmetry of intraocular pressure
in dataset: phenotype

Hypocalciuria [hp:0003127]
type: SIO_010056
comment: Phenotype [hp:0003127] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypocalciuria
in dataset: phenotype

Decreased cervical spine flexion due to contractures of posterior cervical muscles [hp:0004631]
type: SIO_010056
comment: Phenotype [hp:0004631] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased cervical spine flexion due to contractures of posterior cervical muscles
in dataset: phenotype

Perianal abscess [hp:0009789]
type: SIO_010056
comment: Phenotype [hp:0009789] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Perianal abscess
in dataset: phenotype

Decreased number of small peripheral myelinated nerve fibers [hp:0007249]
type: SIO_010056
comment: Phenotype [hp:0007249] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased number of small peripheral myelinated nerve fibers
in dataset: phenotype

Metatarsal synostosis [hp:0001440]
type: SIO_010056
comment: Phenotype [hp:0001440] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metatarsal synostosis
in dataset: phenotype

Hypoventilation [hp:0002791]
type: SIO_010056
comment: Phenotype [hp:0002791] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoventilation
in dataset: phenotype

Abnormality of the amniotic fluid [hp:0001560]
type: SIO_010056
comment: Phenotype [hp:0001560] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the amniotic fluid
in dataset: phenotype

Increased connective tissue [hp:0009025]
type: SIO_010056
comment: Phenotype [hp:0009025] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased connective tissue
in dataset: phenotype

Abnormality of the lymphatic system [hp:0100763]
type: SIO_010056
comment: Phenotype [hp:0100763] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the lymphatic system
in dataset: phenotype

Tachycardia (with pheochromocytoma) [hp:0001673]
type: SIO_010056
comment: Phenotype [hp:0001673] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tachycardia (with pheochromocytoma)
in dataset: phenotype

Hypochromic anemia [hp:0001931]
type: SIO_010056
comment: Phenotype [hp:0001931] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypochromic anemia
in dataset: phenotype

Dacrocystitis [hp:0000620]
type: SIO_010056
comment: Phenotype [hp:0000620] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dacrocystitis
in dataset: phenotype

Bimanual synkinesia [hp:0001335]
type: SIO_010056
comment: Phenotype [hp:0001335] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bimanual synkinesia
in dataset: phenotype

Cholesterol gallstones [hp:0011980]
type: SIO_010056
comment: Phenotype [hp:0011980] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cholesterol gallstones
in dataset: phenotype

Progressive fusion 2nd-5th pip joints [hp:0006147]
type: SIO_010056
comment: Phenotype [hp:0006147] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive fusion 2nd-5th pip joints
in dataset: phenotype

Tritanomaly [hp:0000552]
type: SIO_010056
comment: Phenotype [hp:0000552] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tritanomaly
in dataset: phenotype

Lipoatrophy [hp:0100578]
type: SIO_010056
comment: Phenotype [hp:0100578] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lipoatrophy
in dataset: phenotype

Paralytic ileus [hp:0002590]
type: SIO_010056
comment: Phenotype [hp:0002590] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paralytic ileus
in dataset: phenotype

Prolonged bleeding after surgery [hp:0004846]
type: SIO_010056
comment: Phenotype [hp:0004846] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolonged bleeding after surgery
in dataset: phenotype

Ornithinuria [hp:0003532]
type: SIO_010056
comment: Phenotype [hp:0003532] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ornithinuria
in dataset: phenotype

High palate [hp:0000218]
type: SIO_010056
comment: Phenotype [hp:0000218] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High palate
in dataset: phenotype

Abnormality of the abdominal wall [hp:0004298]
type: SIO_010056
comment: Phenotype [hp:0004298] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the abdominal wall
in dataset: phenotype

Moyamoya phenomenon [hp:0011834]
type: SIO_010056
comment: Phenotype [hp:0011834] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Moyamoya phenomenon
in dataset: phenotype

Absent fifth fingernail [hp:0200104]
type: SIO_010056
comment: Phenotype [hp:0200104] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent fifth fingernail
in dataset: phenotype

Cochlear degeneration [hp:0005102]
type: SIO_010056
comment: Phenotype [hp:0005102] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cochlear degeneration
in dataset: phenotype

Lateral displacement of the femoral head [hp:0006453]
type: SIO_010056
comment: Phenotype [hp:0006453] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lateral displacement of the femoral head
in dataset: phenotype

Cervical segmentation defect [hp:0004632]
type: SIO_010056
comment: Phenotype [hp:0004632] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cervical segmentation defect
in dataset: phenotype

Dialeptic seizures [hp:0011146]
type: SIO_010056
comment: Phenotype [hp:0011146] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dialeptic seizures
in dataset: phenotype

Premature loss of permanent teeth [hp:0006357]
type: SIO_010056
comment: Phenotype [hp:0006357] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature loss of permanent teeth
in dataset: phenotype

Long upper eyelashes [hp:0007840]
type: SIO_010056
comment: Phenotype [hp:0007840] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long upper eyelashes
in dataset: phenotype

Low-molecular-weight proteinuria [hp:0003126]
type: SIO_010056
comment: Phenotype [hp:0003126] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low-molecular-weight proteinuria
in dataset: phenotype

Neonatal breathing dysregulation [hp:0002790]
type: SIO_010056
comment: Phenotype [hp:0002790] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neonatal breathing dysregulation
in dataset: phenotype

Paroxysmal dyskinesia [hp:0007166]
type: SIO_010056
comment: Phenotype [hp:0007166] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paroxysmal dyskinesia
in dataset: phenotype

Quadriceps aplasia [hp:0009788]
type: SIO_010056
comment: Phenotype [hp:0009788] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Quadriceps aplasia
in dataset: phenotype

Neoplasm of the eye [hp:0100012]
type: SIO_010056
comment: Phenotype [hp:0100012] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the eye
in dataset: phenotype

Nonketotic hyperglycinemia [hp:0008288]
type: SIO_010056
comment: Phenotype [hp:0008288] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonketotic hyperglycinemia
in dataset: phenotype

Polyhydramnios [hp:0001561]
type: SIO_010056
comment: Phenotype [hp:0001561] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polyhydramnios
in dataset: phenotype

Broad philtrum [hp:0000289]
type: SIO_010056
comment: Phenotype [hp:0000289] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad philtrum
in dataset: phenotype

Hemobilia [hp:0100762]
type: SIO_010056
comment: Phenotype [hp:0100762] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemobilia
in dataset: phenotype

Nonspherocytic hemolytic anemia [hp:0001930]
type: SIO_010056
comment: Phenotype [hp:0001930] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonspherocytic hemolytic anemia
in dataset: phenotype

Hypoplasia of latissimus dorsi muscle [hp:0009026]
type: SIO_010056
comment: Phenotype [hp:0009026] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of latissimus dorsi muscle
in dataset: phenotype

Complete atrioventricular canal defect [hp:0001674]
type: SIO_010056
comment: Phenotype [hp:0001674] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Complete atrioventricular canal defect
in dataset: phenotype

Chylothorax [hp:0010310]
type: SIO_010056
comment: Phenotype [hp:0010310] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chylothorax
in dataset: phenotype

Polyphagia [hp:0002591]
type: SIO_010056
comment: Phenotype [hp:0002591] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polyphagia
in dataset: phenotype

Bulbar signs [hp:0002483]
type: SIO_010056
comment: Phenotype [hp:0002483] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bulbar signs
in dataset: phenotype

Communicating hydrocephalus [hp:0001334]
type: SIO_010056
comment: Phenotype [hp:0001334] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Communicating hydrocephalus
in dataset: phenotype

Broad metacarpal epiphyses [hp:0006146]
type: SIO_010056
comment: Phenotype [hp:0006146] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad metacarpal epiphyses
in dataset: phenotype

Mucosal telangiectasiae [hp:0100579]
type: SIO_010056
comment: Phenotype [hp:0100579] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mucosal telangiectasiae
in dataset: phenotype

Foam cells with lamellar inclusion bodies [hp:0003609]
type: SIO_010056
comment: Phenotype [hp:0003609] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Foam cells with lamellar inclusion bodies
in dataset: phenotype

Renal artery stenosis [hp:0001920]
type: SIO_010056
comment: Phenotype [hp:0001920] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal artery stenosis
in dataset: phenotype

Mandibular aplasia [hp:0009939]
type: SIO_010056
comment: Phenotype [hp:0009939] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mandibular aplasia
in dataset: phenotype

Widely-spaced maxillary central incisors [hp:0001566]
type: SIO_010056
comment: Phenotype [hp:0001566] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Widely-spaced maxillary central incisors
in dataset: phenotype

Aplasia of the proximal phalanges of the hand [hp:0010242]
type: SIO_010056
comment: Phenotype [hp:0010242] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the proximal phalanges of the hand
in dataset: phenotype

Amaurosis fugax [hp:0100576]
type: SIO_010056
comment: Phenotype [hp:0100576] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Amaurosis fugax
in dataset: phenotype

Abnormal hand bone ossification [hp:0010660]
type: SIO_010056
comment: Phenotype [hp:0010660] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal hand bone ossification
in dataset: phenotype

Abnormality of the cardiac septa [hp:0001671]
type: SIO_010056
comment: Phenotype [hp:0001671] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the cardiac septa
in dataset: phenotype

Paraganglioma-related cranial nerve palsy [hp:0002377]
type: SIO_010056
comment: Phenotype [hp:0002377] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paraganglioma-related cranial nerve palsy
in dataset: phenotype

Type 1 and type 2 muscle fiber minicore regions [hp:0003787]
type: SIO_010056
comment: Phenotype [hp:0003787] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type 1 and type 2 muscle fiber minicore regions
in dataset: phenotype

Peripapillary chorioretinal atrophy [hp:0007950]
type: SIO_010056
comment: Phenotype [hp:0007950] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripapillary chorioretinal atrophy
in dataset: phenotype

Lipid accumulation in hepatocytes [hp:0006561]
type: SIO_010056
comment: Phenotype [hp:0006561] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lipid accumulation in hepatocytes
in dataset: phenotype

Precocious puberty [hp:0000826]
type: SIO_010056
comment: Phenotype [hp:0000826] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Precocious puberty
in dataset: phenotype

Morbilliform rash [hp:0012282]
type: SIO_010056
comment: Phenotype [hp:0012282] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Morbilliform rash
in dataset: phenotype

Recurrent bronchitis [hp:0002837]
type: SIO_010056
comment: Phenotype [hp:0002837] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent bronchitis
in dataset: phenotype

Hypophosphatemic rickets [hp:0004912]
type: SIO_010056
comment: Phenotype [hp:0004912] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypophosphatemic rickets
in dataset: phenotype

Mandibular osteomyelitis [hp:0007626]
type: SIO_010056
comment: Phenotype [hp:0007626] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mandibular osteomyelitis
in dataset: phenotype

Abnormal nasal morphology [hp:0005105]
type: SIO_010056
comment: Phenotype [hp:0005105] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal nasal morphology
in dataset: phenotype

Subcutaneous hemorrhage [hp:0001933]
type: SIO_010056
comment: Phenotype [hp:0001933] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subcutaneous hemorrhage
in dataset: phenotype

Hypergalactosemia [hp:0012024]
type: SIO_010056
comment: Phenotype [hp:0012024] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypergalactosemia
in dataset: phenotype

Urethral atresia [hp:0000068]
type: SIO_010056
comment: Phenotype [hp:0000068] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urethral atresia
in dataset: phenotype

Sunken cheeks [hp:0009938]
type: SIO_010056
comment: Phenotype [hp:0009938] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sunken cheeks
in dataset: phenotype

Urinary bladder inflammation [hp:0100577]
type: SIO_010056
comment: Phenotype [hp:0100577] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urinary bladder inflammation
in dataset: phenotype

Dystonia [hp:0001332]
type: SIO_010056
comment: Phenotype [hp:0001332] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dystonia
in dataset: phenotype

Upper limb amyotrophy [hp:0009129]
type: SIO_010056
comment: Phenotype [hp:0009129] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Upper limb amyotrophy
in dataset: phenotype

Hypoplastic vertebral bodies [hp:0008479]
type: SIO_010056
comment: Phenotype [hp:0008479] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic vertebral bodies
in dataset: phenotype

Anhidrosis [hp:0000970]
type: SIO_010056
comment: Phenotype [hp:0000970] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anhidrosis
in dataset: phenotype

Developmental regression [hp:0002376]
type: SIO_010056
comment: Phenotype [hp:0002376] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Developmental regression
in dataset: phenotype

Hyperinsulinemic hypoglycemia [hp:0000825]
type: SIO_010056
comment: Phenotype [hp:0000825] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperinsulinemic hypoglycemia
in dataset: phenotype

Pulmonary hypoplasia [hp:0002089]
type: SIO_010056
comment: Phenotype [hp:0002089] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary hypoplasia
in dataset: phenotype

Small distal femoral epiphysis [hp:0012283]
type: SIO_010056
comment: Phenotype [hp:0012283] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small distal femoral epiphysis
in dataset: phenotype

Hypoplastic nasal septum [hp:0005104]
type: SIO_010056
comment: Phenotype [hp:0005104] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic nasal septum
in dataset: phenotype

Hypochromic microcytic anemia [hp:0004840]
type: SIO_010056
comment: Phenotype [hp:0004840] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypochromic microcytic anemia
in dataset: phenotype

Peripheral axonal neuropathy [hp:0003477]
type: SIO_010056
comment: Phenotype [hp:0003477] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral axonal neuropathy
in dataset: phenotype

Aplasia of the testes [hp:0010469]
type: SIO_010056
comment: Phenotype [hp:0010469] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the testes
in dataset: phenotype

Intermittent lactic acidemia [hp:0004913]
type: SIO_010056
comment: Phenotype [hp:0004913] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intermittent lactic acidemia
in dataset: phenotype

Sepsis [hp:0100806]
type: SIO_010056
comment: Phenotype [hp:0100806] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sepsis
in dataset: phenotype

Increased serum iduronate sulfatase activity [hp:0003538]
type: SIO_010056
comment: Phenotype [hp:0003538] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased serum iduronate sulfatase activity
in dataset: phenotype

Periorbital fullness [hp:0000629]
type: SIO_010056
comment: Phenotype [hp:0000629] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Periorbital fullness
in dataset: phenotype

Acral ulceration and osteomyelitis leading to autoamputation of the digits (feet) [hp:0001862]
type: SIO_010056
comment: Phenotype [hp:0001862] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acral ulceration and osteomyelitis leading to autoamputation of the digits (feet)
in dataset: phenotype

Uncombable hair [hp:0030056]
type: SIO_010056
comment: Phenotype [hp:0030056] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Uncombable hair
in dataset: phenotype

Biliary tract neoplasm [hp:0100574]
type: SIO_010056
comment: Phenotype [hp:0100574] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Biliary tract neoplasm
in dataset: phenotype

Thoracic scoliosis [hp:0002943]
type: SIO_010056
comment: Phenotype [hp:0002943] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thoracic scoliosis
in dataset: phenotype

Absent septum pellucidum [hp:0001331]
type: SIO_010056
comment: Phenotype [hp:0001331] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent septum pellucidum
in dataset: phenotype

Autosomal dominant somatic cell mutation [hp:0001444]
type: SIO_010056
comment: Phenotype [hp:0001444] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autosomal dominant somatic cell mutation
in dataset: phenotype

Scissor gait [hp:0012407]
type: SIO_010056
comment: Phenotype [hp:0012407] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scissor gait
in dataset: phenotype

Hypokinesia [hp:0002375]
type: SIO_010056
comment: Phenotype [hp:0002375] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypokinesia
in dataset: phenotype

Abnormality of the ureter [hp:0000069]
type: SIO_010056
comment: Phenotype [hp:0000069] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the ureter
in dataset: phenotype

Facial hirsutism [hp:0009937]
type: SIO_010056
comment: Phenotype [hp:0009937] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial hirsutism
in dataset: phenotype

Hyporeflexia of lower limbs [hp:0002600]
type: SIO_010056
comment: Phenotype [hp:0002600] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyporeflexia of lower limbs
in dataset: phenotype

Map-dot-fingerprint corneal dystrophy [hp:0007690]
type: SIO_010056
comment: Phenotype [hp:0007690] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Map-dot-fingerprint corneal dystrophy
in dataset: phenotype

Poor fine motor coordination [hp:0007010]
type: SIO_010056
comment: Phenotype [hp:0007010] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poor fine motor coordination
in dataset: phenotype

Minicore (multicore) myopathy [hp:0003789]
type: SIO_010056
comment: Phenotype [hp:0003789] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Minicore (multicore) myopathy
in dataset: phenotype

Abnormally folded helix [hp:0008544]
type: SIO_010056
comment: Phenotype [hp:0008544] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormally folded helix
in dataset: phenotype

Fragmented epiphyses [hp:0100168]
type: SIO_010056
comment: Phenotype [hp:0100168] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fragmented epiphyses
in dataset: phenotype

Abnormality of the diencephalon [hp:0010662]
type: SIO_010056
comment: Phenotype [hp:0010662] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the diencephalon
in dataset: phenotype

Hepatic amyloidosis [hp:0012280]
type: SIO_010056
comment: Phenotype [hp:0012280] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatic amyloidosis
in dataset: phenotype

Malformation of the hepatic ductal plate [hp:0006563]
type: SIO_010056
comment: Phenotype [hp:0006563] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malformation of the hepatic ductal plate
in dataset: phenotype

Enlarged interphalangeal joints [hp:0006247]
type: SIO_010056
comment: Phenotype [hp:0006247] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged interphalangeal joints
in dataset: phenotype

Growth hormone deficiency [hp:0000824]
type: SIO_010056
comment: Phenotype [hp:0000824] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Growth hormone deficiency
in dataset: phenotype

Mandibular condyle hypoplasia [hp:0007628]
type: SIO_010056
comment: Phenotype [hp:0007628] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mandibular condyle hypoplasia
in dataset: phenotype

Renal corticomedullary cysts [hp:0000108]
type: SIO_010056
comment: Phenotype [hp:0000108] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal corticomedullary cysts
in dataset: phenotype

Vacuolated lymphocytes [hp:0001922]
type: SIO_010056
comment: Phenotype [hp:0001922] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vacuolated lymphocytes
in dataset: phenotype

Hypouricemia [hp:0003537]
type: SIO_010056
comment: Phenotype [hp:0003537] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypouricemia
in dataset: phenotype

Abnormality of the sacrum [hp:0005107]
type: SIO_010056
comment: Phenotype [hp:0005107] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the sacrum
in dataset: phenotype

Microcytic anemia [hp:0001935]
type: SIO_010056
comment: Phenotype [hp:0001935] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microcytic anemia
in dataset: phenotype

Aspiration [hp:0002835]
type: SIO_010056
comment: Phenotype [hp:0002835] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aspiration
in dataset: phenotype

Long fingers [hp:0100807]
type: SIO_010056
comment: Phenotype [hp:0100807] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long fingers
in dataset: phenotype

Reduced factor XII activity [hp:0004841]
type: SIO_010056
comment: Phenotype [hp:0004841] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced factor XII activity
in dataset: phenotype

Impairment of galactose metabolism [hp:0004915]
type: SIO_010056
comment: Phenotype [hp:0004915] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impairment of galactose metabolism
in dataset: phenotype

Short proximal phalanx of finger [hp:0010241]
type: SIO_010056
comment: Phenotype [hp:0010241] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short proximal phalanx of finger
in dataset: phenotype

Corneal dystrophy [hp:0001131]
type: SIO_010056
comment: Phenotype [hp:0001131] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corneal dystrophy
in dataset: phenotype

Autoimmune antibody positivity [hp:0030057]
type: SIO_010056
comment: Phenotype [hp:0030057] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autoimmune antibody positivity
in dataset: phenotype

Thoracic kyphosis [hp:0002942]
type: SIO_010056
comment: Phenotype [hp:0002942] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thoracic kyphosis
in dataset: phenotype

Abnormality of thalamus morphology [hp:0010663]
type: SIO_010056
comment: Phenotype [hp:0010663] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of thalamus morphology
in dataset: phenotype

Asymmetric septal hypertrophy [hp:0001670]
type: SIO_010056
comment: Phenotype [hp:0001670] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Asymmetric septal hypertrophy
in dataset: phenotype

Chylous ascites [hp:0012281]
type: SIO_010056
comment: Phenotype [hp:0012281] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chylous ascites
in dataset: phenotype

Viral hepatitis [hp:0006562]
type: SIO_010056
comment: Phenotype [hp:0006562] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Viral hepatitis
in dataset: phenotype

Delayed puberty [hp:0000823]
type: SIO_010056
comment: Phenotype [hp:0000823] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed puberty
in dataset: phenotype

Galactosuria [hp:0012023]
type: SIO_010056
comment: Phenotype [hp:0012023] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Galactosuria
in dataset: phenotype

Reticulocytosis [hp:0001923]
type: SIO_010056
comment: Phenotype [hp:0001923] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reticulocytosis
in dataset: phenotype

Biconcave vertebral bodies [hp:0004586]
type: SIO_010056
comment: Phenotype [hp:0004586] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Biconcave vertebral bodies
in dataset: phenotype

Pulmonary infiltrates [hp:0002113]
type: SIO_010056
comment: Phenotype [hp:0002113] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary infiltrates
in dataset: phenotype

Limited wrist movement [hp:0006248]
type: SIO_010056
comment: Phenotype [hp:0006248] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited wrist movement
in dataset: phenotype

Abnormality of the helix [hp:0011039]
type: SIO_010056
comment: Phenotype [hp:0011039] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the helix
in dataset: phenotype

Bilateral intracranial calcifications [hp:0005671]
type: SIO_010056
comment: Phenotype [hp:0005671] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral intracranial calcifications
in dataset: phenotype

Mandibular condyle aplasia [hp:0007627]
type: SIO_010056
comment: Phenotype [hp:0007627] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mandibular condyle aplasia
in dataset: phenotype

Bifid sternum [hp:0010309]
type: SIO_010056
comment: Phenotype [hp:0010309] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid sternum
in dataset: phenotype

Persistent bleeding after trauma [hp:0001934]
type: SIO_010056
comment: Phenotype [hp:0001934] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Persistent bleeding after trauma
in dataset: phenotype

Decreased fumarate hydratase activity [hp:0003536]
type: SIO_010056
comment: Phenotype [hp:0003536] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased fumarate hydratase activity
in dataset: phenotype

Bladder exstrophy [hp:0002836]
type: SIO_010056
comment: Phenotype [hp:0002836] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bladder exstrophy
in dataset: phenotype

Abnormality of the vertebral endplates [hp:0005106]
type: SIO_010056
comment: Phenotype [hp:0005106] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the vertebral endplates
in dataset: phenotype

Multiple mitochondrial DNA deletions [hp:0003689]
type: SIO_010056
comment: Phenotype [hp:0003689] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple mitochondrial DNA deletions
in dataset: phenotype

Medial rotation of the medial malleolus [hp:0008132]
type: SIO_010056
comment: Phenotype [hp:0008132] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Medial rotation of the medial malleolus
in dataset: phenotype

Irregular sclerotic endplates [hp:0008476]
type: SIO_010056
comment: Phenotype [hp:0008476] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular sclerotic endplates
in dataset: phenotype

Hyperhidrosis [hp:0000975]
type: SIO_010056
comment: Phenotype [hp:0000975] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperhidrosis
in dataset: phenotype

Synostosis involving bones of the fingers [hp:0009700]
type: SIO_010056
comment: Phenotype [hp:0009700] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Synostosis involving bones of the fingers
in dataset: phenotype

Thick hair [hp:0100874]
type: SIO_010056
comment: Phenotype [hp:0100874] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thick hair
in dataset: phenotype

Trident hand [hp:0004060]
type: SIO_010056
comment: Phenotype [hp:0004060] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Trident hand
in dataset: phenotype

Febrile seizures [hp:0002373]
type: SIO_010056
comment: Phenotype [hp:0002373] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Febrile seizures
in dataset: phenotype

Albinism [hp:0001022]
type: SIO_010056
comment: Phenotype [hp:0001022] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Albinism
in dataset: phenotype

Hypocitraturia [hp:0012405]
type: SIO_010056
comment: Phenotype [hp:0012405] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypocitraturia
in dataset: phenotype

Externally rotated/abducted legs [hp:0003783]
type: SIO_010056
comment: Phenotype [hp:0003783] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Externally rotated/abducted legs
in dataset: phenotype

Cystic angiomatosis of bone [hp:0002833]
type: SIO_010056
comment: Phenotype [hp:0002833] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cystic angiomatosis of bone
in dataset: phenotype

Generalized distal tubular acidosis [hp:0004916]
type: SIO_010056
comment: Phenotype [hp:0004916] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized distal tubular acidosis
in dataset: phenotype

Perifollicular hyperkeratosis [hp:0007468]
type: SIO_010056
comment: Phenotype [hp:0007468] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Perifollicular hyperkeratosis
in dataset: phenotype

Thick lower lip vermilion [hp:0000179]
type: SIO_010056
comment: Phenotype [hp:0000179] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thick lower lip vermilion
in dataset: phenotype

Malrotation of colon [hp:0004785]
type: SIO_010056
comment: Phenotype [hp:0004785] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malrotation of colon
in dataset: phenotype

Hepatocellular adenoma [hp:0012028]
type: SIO_010056
comment: Phenotype [hp:0012028] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatocellular adenoma
in dataset: phenotype

Sideroblastic anemia [hp:0001924]
type: SIO_010056
comment: Phenotype [hp:0001924] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sideroblastic anemia
in dataset: phenotype

Intervertebral space narrowing [hp:0002945]
type: SIO_010056
comment: Phenotype [hp:0002945] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intervertebral space narrowing
in dataset: phenotype

Microangiopathic hemolytic anemia [hp:0001937]
type: SIO_010056
comment: Phenotype [hp:0001937] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microangiopathic hemolytic anemia
in dataset: phenotype

Decreased activity of cytochrome C oxidase in muscle tissue [hp:0003688]
type: SIO_010056
comment: Phenotype [hp:0003688] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased activity of cytochrome C oxidase in muscle tissue
in dataset: phenotype

Hypertension [hp:0000822]
type: SIO_010056
comment: Phenotype [hp:0000822] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertension
in dataset: phenotype

Abnormality of the respiratory system [hp:0002086]
type: SIO_010056
comment: Phenotype [hp:0002086] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the respiratory system
in dataset: phenotype

Abnormal hypothalamus morphology [hp:0012286]
type: SIO_010056
comment: Phenotype [hp:0012286] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal hypothalamus morphology
in dataset: phenotype

Increased hepatocellular lipid droplets [hp:0006565]
type: SIO_010056
comment: Phenotype [hp:0006565] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased hepatocellular lipid droplets
in dataset: phenotype

Sensory impairment [hp:0003474]
type: SIO_010056
comment: Phenotype [hp:0003474] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sensory impairment
in dataset: phenotype

Tarsal stippling [hp:0008131]
type: SIO_010056
comment: Phenotype [hp:0008131] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tarsal stippling
in dataset: phenotype

Papilloma [hp:0012740]
type: SIO_010056
comment: Phenotype [hp:0012740] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Papilloma
in dataset: phenotype

Decreased cervical spine mobility [hp:0004637]
type: SIO_010056
comment: Phenotype [hp:0004637] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased cervical spine mobility
in dataset: phenotype

Distal tapering of metatarsals [hp:0008133]
type: SIO_010056
comment: Phenotype [hp:0008133] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal tapering of metatarsals
in dataset: phenotype

Bilateral coxa valga [hp:0010665]
type: SIO_010056
comment: Phenotype [hp:0010665] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral coxa valga
in dataset: phenotype

Metacarpal synostosis [hp:0009701]
type: SIO_010056
comment: Phenotype [hp:0009701] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metacarpal synostosis
in dataset: phenotype

Hypothyroidism [hp:0000821]
type: SIO_010056
comment: Phenotype [hp:0000821] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypothyroidism
in dataset: phenotype

Hyperextensible skin [hp:0000974]
type: SIO_010056
comment: Phenotype [hp:0000974] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperextensible skin
in dataset: phenotype

Hypoplastic sacral vertebrae [hp:0008475]
type: SIO_010056
comment: Phenotype [hp:0008475] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic sacral vertebrae
in dataset: phenotype

Eunuchoid habitus [hp:0003782]
type: SIO_010056
comment: Phenotype [hp:0003782] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Eunuchoid habitus
in dataset: phenotype

Thoracolumbar scoliosis [hp:0002944]
type: SIO_010056
comment: Phenotype [hp:0002944] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thoracolumbar scoliosis
in dataset: phenotype

Normal interictal EEG [hp:0002372]
type: SIO_010056
comment: Phenotype [hp:0002372] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Normal interictal EEG
in dataset: phenotype

Abnormality of lower lip [hp:0000178]
type: SIO_010056
comment: Phenotype [hp:0000178] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of lower lip
in dataset: phenotype

Obsessive-compulsive trait [hp:0008770]
type: SIO_010056
comment: Phenotype [hp:0008770] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Obsessive-compulsive trait
in dataset: phenotype

Absent urinary urothione [hp:0003606]
type: SIO_010056
comment: Phenotype [hp:0003606] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent urinary urothione
in dataset: phenotype

Flared femoral metaphysis [hp:0002834]
type: SIO_010056
comment: Phenotype [hp:0002834] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flared femoral metaphysis
in dataset: phenotype

Dorsal subluxation of ulna [hp:0006459]
type: SIO_010056
comment: Phenotype [hp:0006459] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dorsal subluxation of ulna
in dataset: phenotype

Ventriculomegaly [hp:0002119]
type: SIO_010056
comment: Phenotype [hp:0002119] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ventriculomegaly
in dataset: phenotype

Ectopic ossification in ligament tissue [hp:0011989]
type: SIO_010056
comment: Phenotype [hp:0011989] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopic ossification in ligament tissue
in dataset: phenotype

Cleft eyelid [hp:0000625]
type: SIO_010056
comment: Phenotype [hp:0000625] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cleft eyelid
in dataset: phenotype

Centrally nucleated skeletal muscle fibers [hp:0003687]
type: SIO_010056
comment: Phenotype [hp:0003687] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Centrally nucleated skeletal muscle fibers
in dataset: phenotype

Abnormality of the intervertebral disk [hp:0005108]
type: SIO_010056
comment: Phenotype [hp:0005108] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the intervertebral disk
in dataset: phenotype

Hypothalamic luteinizing hormone-releasing hormone deficiency [hp:0012287]
type: SIO_010056
comment: Phenotype [hp:0012287] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypothalamic luteinizing hormone-releasing hormone deficiency
in dataset: phenotype

Stridor [hp:0010307]
type: SIO_010056
comment: Phenotype [hp:0010307] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stridor
in dataset: phenotype

Generalized morning stiffness [hp:0005197]
type: SIO_010056
comment: Phenotype [hp:0005197] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized morning stiffness
in dataset: phenotype

Telangiectasia of extensor surfaces [hp:0007621]
type: SIO_010056
comment: Phenotype [hp:0007621] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Telangiectasia of extensor surfaces
in dataset: phenotype

Fluctuating hepatomegaly [hp:0006564]
type: SIO_010056
comment: Phenotype [hp:0006564] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fluctuating hepatomegaly
in dataset: phenotype

Juvenile gastrointestinal polyposis [hp:0004784]
type: SIO_010056
comment: Phenotype [hp:0004784] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Juvenile gastrointestinal polyposis
in dataset: phenotype

Fatigable weakness [hp:0003473]
type: SIO_010056
comment: Phenotype [hp:0003473] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fatigable weakness
in dataset: phenotype

Occipital encephalocele [hp:0002085]
type: SIO_010056
comment: Phenotype [hp:0002085] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Occipital encephalocele
in dataset: phenotype

Decreased CSF homovanillic acid (HVA) [hp:0003785]
type: SIO_010056
comment: Phenotype [hp:0003785] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased CSF homovanillic acid (HVA)
in dataset: phenotype

Anterior radial head dislocation [hp:0005084]
type: SIO_010056
comment: Phenotype [hp:0005084] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior radial head dislocation
in dataset: phenotype

Cutis laxa [hp:0000973]
type: SIO_010056
comment: Phenotype [hp:0000973] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cutis laxa
in dataset: phenotype

Abnormality of the thyroid gland [hp:0000820]
type: SIO_010056
comment: Phenotype [hp:0000820] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the thyroid gland
in dataset: phenotype

Carcinoid tumor [hp:0100570]
type: SIO_010056
comment: Phenotype [hp:0100570] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Carcinoid tumor
in dataset: phenotype

Elevated amniotic fluid alpha-fetoprotein [hp:0004639]
type: SIO_010056
comment: Phenotype [hp:0004639] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated amniotic fluid alpha-fetoprotein
in dataset: phenotype

Abnormality of the scapula [hp:0000782]
type: SIO_010056
comment: Phenotype [hp:0000782] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the scapula
in dataset: phenotype

Irregular tarsal ossification [hp:0008134]
type: SIO_010056
comment: Phenotype [hp:0008134] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular tarsal ossification
in dataset: phenotype

Scheuermann-like vertebral changes [hp:0008478]
type: SIO_010056
comment: Phenotype [hp:0008478] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scheuermann-like vertebral changes
in dataset: phenotype

Narrow naris [hp:0009933]
type: SIO_010056
comment: Phenotype [hp:0009933] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow naris
in dataset: phenotype

Long coccyx [hp:0002831]
type: SIO_010056
comment: Phenotype [hp:0002831] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long coccyx
in dataset: phenotype

4-Hydroxyphenylacetic aciduria [hp:0003607]
type: SIO_010056
comment: Phenotype [hp:0003607] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 4-Hydroxyphenylacetic aciduria
in dataset: phenotype

Loss of speech [hp:0002371]
type: SIO_010056
comment: Phenotype [hp:0002371] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Loss of speech
in dataset: phenotype

Infra-orbital crease [hp:0100876]
type: SIO_010056
comment: Phenotype [hp:0100876] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Infra-orbital crease
in dataset: phenotype

Hyperchloremic metabolic acidosis [hp:0004918]
type: SIO_010056
comment: Phenotype [hp:0004918] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperchloremic metabolic acidosis
in dataset: phenotype

Hyperornithinemia [hp:0012026]
type: SIO_010056
comment: Phenotype [hp:0012026] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperornithinemia
in dataset: phenotype

Abnormality of metabolism/homeostasis [hp:0001939]
type: SIO_010056
comment: Phenotype [hp:0001939] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of metabolism/homeostasis
in dataset: phenotype

Short thorax [hp:0010306]
type: SIO_010056
comment: Phenotype [hp:0010306] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short thorax
in dataset: phenotype

Cervical kyphosis [hp:0002947]
type: SIO_010056
comment: Phenotype [hp:0002947] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cervical kyphosis
in dataset: phenotype

Multicentric ossification of proximal humeral epiphyses [hp:0004997]
type: SIO_010056
comment: Phenotype [hp:0004997] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multicentric ossification of proximal humeral epiphyses
in dataset: phenotype

Ectopic ossification in tendon tissue [hp:0011988]
type: SIO_010056
comment: Phenotype [hp:0011988] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopic ossification in tendon tissue
in dataset: phenotype

Encephalocele [hp:0002084]
type: SIO_010056
comment: Phenotype [hp:0002084] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Encephalocele
in dataset: phenotype

Hypocalcemic tetany [hp:0003472]
type: SIO_010056
comment: Phenotype [hp:0003472] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypocalcemic tetany
in dataset: phenotype

Duodenal polyposis [hp:0004783]
type: SIO_010056
comment: Phenotype [hp:0004783] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Duodenal polyposis
in dataset: phenotype

Iliac horns [hp:0009780]
type: SIO_010056
comment: Phenotype [hp:0009780] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Iliac horns
in dataset: phenotype

Limited knee flexion/extension [hp:0005085]
type: SIO_010056
comment: Phenotype [hp:0005085] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited knee flexion/extension
in dataset: phenotype

Stiff interphalangeal joints [hp:0005198]
type: SIO_010056
comment: Phenotype [hp:0005198] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stiff interphalangeal joints
in dataset: phenotype

Nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic) [hp:0003809]
type: SIO_010056
comment: Phenotype [hp:0003809] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic)
in dataset: phenotype

Small proximal tibial epiphyses [hp:0012284]
type: SIO_010056
comment: Phenotype [hp:0012284] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small proximal tibial epiphyses
in dataset: phenotype

Abnormal pupillary light reflex [hp:0007695]
type: SIO_010056
comment: Phenotype [hp:0007695] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal pupillary light reflex
in dataset: phenotype

Palmoplantar hyperkeratosis [hp:0000972]
type: SIO_010056
comment: Phenotype [hp:0000972] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palmoplantar hyperkeratosis
in dataset: phenotype

Type 1 collagen overmodification [hp:0003784]
type: SIO_010056
comment: Phenotype [hp:0003784] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type 1 collagen overmodification
in dataset: phenotype

Palmoplantar cutis gyrata [hp:0007469]
type: SIO_010056
comment: Phenotype [hp:0007469] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palmoplantar cutis gyrata
in dataset: phenotype

Poorly ossified cervical vertebrae [hp:0008477]
type: SIO_010056
comment: Phenotype [hp:0008477] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poorly ossified cervical vertebrae
in dataset: phenotype

Single naris [hp:0009932]
type: SIO_010056
comment: Phenotype [hp:0009932] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Single naris
in dataset: phenotype

Poor coordination [hp:0002370]
type: SIO_010056
comment: Phenotype [hp:0002370] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poor coordination
in dataset: phenotype

Calcific stippling [hp:0002832]
type: SIO_010056
comment: Phenotype [hp:0002832] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcific stippling
in dataset: phenotype

Submucous cleft hard palate [hp:0000176]
type: SIO_010056
comment: Phenotype [hp:0000176] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Submucous cleft hard palate
in dataset: phenotype

Underdeveloped antitragus [hp:0011251]
type: SIO_010056
comment: Phenotype [hp:0011251] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Underdeveloped antitragus
in dataset: phenotype

Supernumerary vertebrae [hp:0002946]
type: SIO_010056
comment: Phenotype [hp:0002946] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Supernumerary vertebrae
in dataset: phenotype

Ungual fibroma [hp:0100804]
type: SIO_010056
comment: Phenotype [hp:0100804] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ungual fibroma
in dataset: phenotype

Ectopic ossification in muscle tissue [hp:0011987]
type: SIO_010056
comment: Phenotype [hp:0011987] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopic ossification in muscle tissue
in dataset: phenotype

Posterior embryotoxon [hp:0000627]
type: SIO_010056
comment: Phenotype [hp:0000627] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior embryotoxon
in dataset: phenotype

Acanthocytosis [hp:0001927]
type: SIO_010056
comment: Phenotype [hp:0001927] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acanthocytosis
in dataset: phenotype

Laryngeal edema [hp:0012027]
type: SIO_010056
comment: Phenotype [hp:0012027] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laryngeal edema
in dataset: phenotype

Pigmentation anomalies of sun-exposed skin [hp:0007623]
type: SIO_010056
comment: Phenotype [hp:0007623] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pigmentation anomalies of sun-exposed skin
in dataset: phenotype

Aplasia/Hypoplasia of the abdominal wall musculature [hp:0010318]
type: SIO_010056
comment: Phenotype [hp:0010318] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the abdominal wall musculature
in dataset: phenotype

Aplasia of the abdominal wall musculature [hp:0005199]
type: SIO_010056
comment: Phenotype [hp:0005199] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the abdominal wall musculature
in dataset: phenotype

Migraine without aura [hp:0002083]
type: SIO_010056
comment: Phenotype [hp:0002083] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Migraine without aura
in dataset: phenotype

Neonatal cholestatic liver disease [hp:0006566]
type: SIO_010056
comment: Phenotype [hp:0006566] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neonatal cholestatic liver disease
in dataset: phenotype

Hypotrichosis of the scalp [hp:0004782]
type: SIO_010056
comment: Phenotype [hp:0004782] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypotrichosis of the scalp
in dataset: phenotype

Knee osteoarthritis [hp:0005086]
type: SIO_010056
comment: Phenotype [hp:0005086] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Knee osteoarthritis
in dataset: phenotype

Retinal pigment epithelial atrophy [hp:0007698]
type: SIO_010056
comment: Phenotype [hp:0007698] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal pigment epithelial atrophy
in dataset: phenotype

Astrocytoma [hp:0009592]
type: SIO_010056
comment: Phenotype [hp:0009592] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Astrocytoma
in dataset: phenotype

Infertility [hp:0000789]
type: SIO_010056
comment: Phenotype [hp:0000789] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Infertility
in dataset: phenotype

Abdominal obesity [hp:0012743]
type: SIO_010056
comment: Phenotype [hp:0012743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abdominal obesity
in dataset: phenotype

Hepatic necrosis [hp:0002605]
type: SIO_010056
comment: Phenotype [hp:0002605] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatic necrosis
in dataset: phenotype

Ventricular hypertrophy [hp:0001714]
type: SIO_010056
comment: Phenotype [hp:0001714] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ventricular hypertrophy
in dataset: phenotype

Echolalia [hp:0010529]
type: SIO_010056
comment: Phenotype [hp:0010529] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Echolalia
in dataset: phenotype

Rectal abscess [hp:0005224]
type: SIO_010056
comment: Phenotype [hp:0005224] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rectal abscess
in dataset: phenotype

Abnormality of coagulation [hp:0001928]
type: SIO_010056
comment: Phenotype [hp:0001928] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of coagulation
in dataset: phenotype

Hyposerinemia [hp:0012279]
type: SIO_010056
comment: Phenotype [hp:0012279] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyposerinemia
in dataset: phenotype

Pericentral retinitis pigmentosa [hp:0007947]
type: SIO_010056
comment: Phenotype [hp:0007947] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pericentral retinitis pigmentosa
in dataset: phenotype

Renal amyloidosis [hp:0001917]
type: SIO_010056
comment: Phenotype [hp:0001917] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal amyloidosis
in dataset: phenotype

Sclerosis of skull base [hp:0002694]
type: SIO_010056
comment: Phenotype [hp:0002694] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sclerosis of skull base
in dataset: phenotype

Polyuria [hp:0000103]
type: SIO_010056
comment: Phenotype [hp:0000103] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polyuria
in dataset: phenotype

Abnormality of the male genitalia [hp:0010461]
type: SIO_010056
comment: Phenotype [hp:0010461] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the male genitalia
in dataset: phenotype

Absent proximal phalanx of thumb [hp:0009637]
type: SIO_010056
comment: Phenotype [hp:0009637] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent proximal phalanx of thumb
in dataset: phenotype

Tip-toe gait [hp:0030051]
type: SIO_010056
comment: Phenotype [hp:0030051] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tip-toe gait
in dataset: phenotype

Eruptive xanthomas [hp:0001013]
type: SIO_010056
comment: Phenotype [hp:0001013] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Eruptive xanthomas
in dataset: phenotype

Slender finger [hp:0001238]
type: SIO_010056
comment: Phenotype [hp:0001238] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slender finger
in dataset: phenotype

Abnormality of the fifth metatarsal bone [hp:0008089]
type: SIO_010056
comment: Phenotype [hp:0008089] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the fifth metatarsal bone
in dataset: phenotype

Intention tremor [hp:0002080]
type: SIO_010056
comment: Phenotype [hp:0002080] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intention tremor
in dataset: phenotype

Hemianopic blurring of vision [hp:0001125]
type: SIO_010056
comment: Phenotype [hp:0001125] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemianopic blurring of vision
in dataset: phenotype

Megacalicosis [hp:0100581]
type: SIO_010056
comment: Phenotype [hp:0100581] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Megacalicosis
in dataset: phenotype

Hydroureter [hp:0000072]
type: SIO_010056
comment: Phenotype [hp:0000072] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hydroureter
in dataset: phenotype

Autonomic dysregulation [hp:0002271]
type: SIO_010056
comment: Phenotype [hp:0002271] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autonomic dysregulation
in dataset: phenotype

Abnormality of the vestibulocochlear nerve [hp:0009591]
type: SIO_010056
comment: Phenotype [hp:0009591] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the vestibulocochlear nerve
in dataset: phenotype

Respiratory insufficiency due to defective ciliary clearance [hp:0200073]
type: SIO_010056
comment: Phenotype [hp:0200073] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Respiratory insufficiency due to defective ciliary clearance
in dataset: phenotype

Forehead hyperpigmentation [hp:0005336]
type: SIO_010056
comment: Phenotype [hp:0005336] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Forehead hyperpigmentation
in dataset: phenotype

Autoamputation (feet) [hp:0001868]
type: SIO_010056
comment: Phenotype [hp:0001868] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autoamputation (feet)
in dataset: phenotype

Tetraamelia [hp:0003057]
type: SIO_010056
comment: Phenotype [hp:0003057] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tetraamelia
in dataset: phenotype

Reduced factor XI activity [hp:0001929]
type: SIO_010056
comment: Phenotype [hp:0001929] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced factor XI activity
in dataset: phenotype

Unilateral narrow palpebral fissure [hp:0007946]
type: SIO_010056
comment: Phenotype [hp:0007946] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral narrow palpebral fissure
in dataset: phenotype

Absent proximal finger flexion creases [hp:0006077]
type: SIO_010056
comment: Phenotype [hp:0006077] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent proximal finger flexion creases
in dataset: phenotype

Broad alveolar ridges [hp:0000187]
type: SIO_010056
comment: Phenotype [hp:0000187] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad alveolar ridges
in dataset: phenotype

Sparse facial hair [hp:0007464]
type: SIO_010056
comment: Phenotype [hp:0007464] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sparse facial hair
in dataset: phenotype

Short proximal phalanx of thumb [hp:0009638]
type: SIO_010056
comment: Phenotype [hp:0009638] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short proximal phalanx of thumb
in dataset: phenotype

Deposits immunoreactive to beta-amyloid protein [hp:0003791]
type: SIO_010056
comment: Phenotype [hp:0003791] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deposits immunoreactive to beta-amyloid protein
in dataset: phenotype

Narcolepsy [hp:0030050]
type: SIO_010056
comment: Phenotype [hp:0030050] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narcolepsy
in dataset: phenotype

Angiokeratoma [hp:0001014]
type: SIO_010056
comment: Phenotype [hp:0001014] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Angiokeratoma
in dataset: phenotype

Ureteral stenosis [hp:0000071]
type: SIO_010056
comment: Phenotype [hp:0000071] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ureteral stenosis
in dataset: phenotype

Barrett esophagus [hp:0100580]
type: SIO_010056
comment: Phenotype [hp:0100580] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Barrett esophagus
in dataset: phenotype

Sleepy facial expression [hp:0005335]
type: SIO_010056
comment: Phenotype [hp:0005335] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sleepy facial expression
in dataset: phenotype

Distal amyotrophy [hp:0003693]
type: SIO_010056
comment: Phenotype [hp:0003693] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal amyotrophy
in dataset: phenotype

Bridged sella turcica [hp:0005449]
type: SIO_010056
comment: Phenotype [hp:0005449] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bridged sella turcica
in dataset: phenotype

Episodic quadriplegia [hp:0200072]
type: SIO_010056
comment: Phenotype [hp:0200072] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic quadriplegia
in dataset: phenotype

Bowel incontinence [hp:0002607]
type: SIO_010056
comment: Phenotype [hp:0002607] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bowel incontinence
in dataset: phenotype

Lipoma of corpus callosum [hp:0006931]
type: SIO_010056
comment: Phenotype [hp:0006931] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lipoma of corpus callosum
in dataset: phenotype

Abnormality of the autonomic nervous system [hp:0002270]
type: SIO_010056
comment: Phenotype [hp:0002270] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the autonomic nervous system
in dataset: phenotype

Retinal hamartoma [hp:0009594]
type: SIO_010056
comment: Phenotype [hp:0009594] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal hamartoma
in dataset: phenotype

Unilateral cryptorchidism [hp:0012741]
type: SIO_010056
comment: Phenotype [hp:0012741] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral cryptorchidism
in dataset: phenotype

Acute kidney injury [hp:0001919]
type: SIO_010056
comment: Phenotype [hp:0001919] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute kidney injury
in dataset: phenotype

Villous atrophy [hp:0011473]
type: SIO_010056
comment: Phenotype [hp:0011473] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Villous atrophy
in dataset: phenotype

Diabetes mellitus [hp:0000819]
type: SIO_010056
comment: Phenotype [hp:0000819] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diabetes mellitus
in dataset: phenotype

Hypoglycinemia [hp:0012277]
type: SIO_010056
comment: Phenotype [hp:0012277] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoglycinemia
in dataset: phenotype

Deep plantar creases [hp:0001869]
type: SIO_010056
comment: Phenotype [hp:0001869] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deep plantar creases
in dataset: phenotype

Wolff-Parkinson-White syndrome [hp:0001716]
type: SIO_010056
comment: Phenotype [hp:0001716] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Wolff-Parkinson-White syndrome
in dataset: phenotype

Bowel diverticulosis [hp:0005222]
type: SIO_010056
comment: Phenotype [hp:0005222] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bowel diverticulosis
in dataset: phenotype

Choroidal degeneration [hp:0007945]
type: SIO_010056
comment: Phenotype [hp:0007945] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Choroidal degeneration
in dataset: phenotype

Cervical spine hypermobility [hp:0003318]
type: SIO_010056
comment: Phenotype [hp:0003318] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cervical spine hypermobility
in dataset: phenotype

Diaphoresis (with pheochromocytoma) [hp:0001011]
type: SIO_010056
comment: Phenotype [hp:0001011] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diaphoresis (with pheochromocytoma)
in dataset: phenotype

Hyperconvex nail [hp:0001795]
type: SIO_010056
comment: Phenotype [hp:0001795] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperconvex nail
in dataset: phenotype

Honeycomb palmoplantar keratoderma [hp:0007465]
type: SIO_010056
comment: Phenotype [hp:0007465] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Honeycomb palmoplantar keratoderma
in dataset: phenotype

Occasional neurofibromas [hp:0009595]
type: SIO_010056
comment: Phenotype [hp:0009595] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Occasional neurofibromas
in dataset: phenotype

Enlarged epiphysis of the proximal phalanx of the 3rd finger [hp:0009349]
type: SIO_010056
comment: Phenotype [hp:0009349] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged epiphysis of the proximal phalanx of the 3rd finger
in dataset: phenotype

Flared humeral metaphysis [hp:0003911]
type: SIO_010056
comment: Phenotype [hp:0003911] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flared humeral metaphysis
in dataset: phenotype

Ureteropelvic junction obstruction [hp:0000074]
type: SIO_010056
comment: Phenotype [hp:0000074] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ureteropelvic junction obstruction
in dataset: phenotype

Bracket epiphysis of the middle phalanx of the 2nd finger [hp:0009514]
type: SIO_010056
comment: Phenotype [hp:0009514] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bracket epiphysis of the middle phalanx of the 2nd finger
in dataset: phenotype

Nephrolithiasis [hp:0000787]
type: SIO_010056
comment: Phenotype [hp:0000787] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nephrolithiasis
in dataset: phenotype

Peripheral vitreoretinal degeneration [hp:0200071]
type: SIO_010056
comment: Phenotype [hp:0200071] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral vitreoretinal degeneration
in dataset: phenotype

Late-onset proximal muscle weakness [hp:0003694]
type: SIO_010056
comment: Phenotype [hp:0003694] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Late-onset proximal muscle weakness
in dataset: phenotype

Yellow nails [hp:0011367]
type: SIO_010056
comment: Phenotype [hp:0011367] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Yellow nails
in dataset: phenotype

Nonossified fifth metatarsal [hp:0008087]
type: SIO_010056
comment: Phenotype [hp:0008087] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonossified fifth metatarsal
in dataset: phenotype

Celiac disease [hp:0002608]
type: SIO_010056
comment: Phenotype [hp:0002608] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Celiac disease
in dataset: phenotype

Frontoparietal cortical dysplasia [hp:0006930]
type: SIO_010056
comment: Phenotype [hp:0006930] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontoparietal cortical dysplasia
in dataset: phenotype

Dysharmonic bone age [hp:0200000]
type: SIO_010056
comment: Phenotype [hp:0200000] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysharmonic bone age
in dataset: phenotype

Peripheral Schwannoma [hp:0009593]
type: SIO_010056
comment: Phenotype [hp:0009593] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral Schwannoma
in dataset: phenotype

Hyperostosis cranialis interna [hp:0005890]
type: SIO_010056
comment: Phenotype [hp:0005890] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperostosis cranialis interna
in dataset: phenotype

Coronary artery calcification [hp:0001717]
type: SIO_010056
comment: Phenotype [hp:0001717] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coronary artery calcification
in dataset: phenotype

Intermittent microsaccadic pursuits [hp:0007944]
type: SIO_010056
comment: Phenotype [hp:0007944] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intermittent microsaccadic pursuits
in dataset: phenotype

Digital flexor tenosynovitis [hp:0012276]
type: SIO_010056
comment: Phenotype [hp:0012276] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Digital flexor tenosynovitis
in dataset: phenotype

Abnormality of the cervical spine [hp:0003319]
type: SIO_010056
comment: Phenotype [hp:0003319] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the cervical spine
in dataset: phenotype

Midfrontal capillary hemangioma [hp:0007466]
type: SIO_010056
comment: Phenotype [hp:0007466] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Midfrontal capillary hemangioma
in dataset: phenotype

Asymmetric, linear skin defects [hp:0007398]
type: SIO_010056
comment: Phenotype [hp:0007398] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Asymmetric, linear skin defects
in dataset: phenotype

Nephrotic syndrome [hp:0000100]
type: SIO_010056
comment: Phenotype [hp:0000100] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nephrotic syndrome
in dataset: phenotype

Cleft soft palate [hp:0000185]
type: SIO_010056
comment: Phenotype [hp:0000185] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cleft soft palate
in dataset: phenotype

Symmetrical, oval parietal bone defects [hp:0002695]
type: SIO_010056
comment: Phenotype [hp:0002695] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Symmetrical, oval parietal bone defects
in dataset: phenotype

Cryptophthalmos [hp:0001126]
type: SIO_010056
comment: Phenotype [hp:0001126] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cryptophthalmos
in dataset: phenotype

Wrist flexion contracture [hp:0001239]
type: SIO_010056
comment: Phenotype [hp:0001239] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Wrist flexion contracture
in dataset: phenotype

Increased nuchal translucency [hp:0010880]
type: SIO_010056
comment: Phenotype [hp:0010880] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased nuchal translucency
in dataset: phenotype

Multiple lipomas [hp:0001012]
type: SIO_010056
comment: Phenotype [hp:0001012] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple lipomas
in dataset: phenotype

Peripheral retinal atrophy [hp:0200070]
type: SIO_010056
comment: Phenotype [hp:0200070] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral retinal atrophy
in dataset: phenotype

Ureteral duplication [hp:0000073]
type: SIO_010056
comment: Phenotype [hp:0000073] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ureteral duplication
in dataset: phenotype

Primary amenorrhea [hp:0000786]
type: SIO_010056
comment: Phenotype [hp:0000786] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Primary amenorrhea
in dataset: phenotype

Renal cyst [hp:0000107]
type: SIO_010056
comment: Phenotype [hp:0000107] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal cyst
in dataset: phenotype

Fine, reticulate skin pigmentation [hp:0007617]
type: SIO_010056
comment: Phenotype [hp:0007617] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fine, reticulate skin pigmentation
in dataset: phenotype

Sensorineural hearing impairment [hp:0000407]
type: SIO_010056
comment: Phenotype [hp:0000407] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sensorineural hearing impairment
in dataset: phenotype

Peripheral dysmyelination [hp:0003469]
type: SIO_010056
comment: Phenotype [hp:0003469] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral dysmyelination
in dataset: phenotype

Generalized myoclonic seizures [hp:0002123]
type: SIO_010056
comment: Phenotype [hp:0002123] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized myoclonic seizures
in dataset: phenotype

Mitral stenosis [hp:0001718]
type: SIO_010056
comment: Phenotype [hp:0001718] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mitral stenosis
in dataset: phenotype

Poor eye contact [hp:0000817]
type: SIO_010056
comment: Phenotype [hp:0000817] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poor eye contact
in dataset: phenotype

Scapular winging [hp:0003691]
type: SIO_010056
comment: Phenotype [hp:0003691] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scapular winging
in dataset: phenotype

Intermittent hyperpnea at rest [hp:0005941]
type: SIO_010056
comment: Phenotype [hp:0005941] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intermittent hyperpnea at rest
in dataset: phenotype

Sacral lipoma [hp:0012033]
type: SIO_010056
comment: Phenotype [hp:0012033] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sacral lipoma
in dataset: phenotype

Optic nerve aplasia [hp:0012521]
type: SIO_010056
comment: Phenotype [hp:0012521] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Optic nerve aplasia
in dataset: phenotype

Severe sensorineural hearing impairment [hp:0008625]
type: SIO_010056
comment: Phenotype [hp:0008625] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe sensorineural hearing impairment
in dataset: phenotype

Paresis of extensor muscles of the big toe [hp:0002601]
type: SIO_010056
comment: Phenotype [hp:0002601] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paresis of extensor muscles of the big toe
in dataset: phenotype

Vesicoureteral reflux [hp:0000076]
type: SIO_010056
comment: Phenotype [hp:0000076] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vesicoureteral reflux
in dataset: phenotype

Aortic valve atresia [hp:0010883]
type: SIO_010056
comment: Phenotype [hp:0010883] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aortic valve atresia
in dataset: phenotype

Anemic pallor [hp:0001017]
type: SIO_010056
comment: Phenotype [hp:0001017] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anemic pallor
in dataset: phenotype

Enlarged epiphysis of the middle phalanx of the 2nd finger [hp:0009516]
type: SIO_010056
comment: Phenotype [hp:0009516] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged epiphysis of the middle phalanx of the 2nd finger
in dataset: phenotype

Toe clinodactyly [hp:0001863]
type: SIO_010056
comment: Phenotype [hp:0001863] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Toe clinodactyly
in dataset: phenotype

Subcutaneous calcification [hp:0007618]
type: SIO_010056
comment: Phenotype [hp:0007618] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subcutaneous calcification
in dataset: phenotype

Dysgraphia [hp:0010526]
type: SIO_010056
comment: Phenotype [hp:0010526] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysgraphia
in dataset: phenotype

Double outlet right ventricle [hp:0001719]
type: SIO_010056
comment: Phenotype [hp:0001719] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Double outlet right ventricle
in dataset: phenotype

Progressive sensorineural hearing impairment [hp:0000408]
type: SIO_010056
comment: Phenotype [hp:0000408] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive sensorineural hearing impairment
in dataset: phenotype

Epiphyseal deformities of tubular bones [hp:0003053]
type: SIO_010056
comment: Phenotype [hp:0003053] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Epiphyseal deformities of tubular bones
in dataset: phenotype

Spider hemangioma [hp:0012522]
type: SIO_010056
comment: Phenotype [hp:0012522] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spider hemangioma
in dataset: phenotype

Abnormality of the endocrine system [hp:0000818]
type: SIO_010056
comment: Phenotype [hp:0000818] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the endocrine system
in dataset: phenotype

Aplasia/Hypoplasia of the lungs [hp:0006703]
type: SIO_010056
comment: Phenotype [hp:0006703] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the lungs
in dataset: phenotype

Lipoma [hp:0012032]
type: SIO_010056
comment: Phenotype [hp:0012032] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lipoma
in dataset: phenotype

Recurrent thrombophlebitis [hp:0004419]
type: SIO_010056
comment: Phenotype [hp:0004419] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent thrombophlebitis
in dataset: phenotype

Low-frequency hearing loss [hp:0008542]
type: SIO_010056
comment: Phenotype [hp:0008542] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low-frequency hearing loss
in dataset: phenotype

Renal duplication [hp:0000075]
type: SIO_010056
comment: Phenotype [hp:0000075] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal duplication
in dataset: phenotype

Parietal foramina [hp:0002697]
type: SIO_010056
comment: Phenotype [hp:0002697] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Parietal foramina
in dataset: phenotype

Pelvic girdle muscle atrophy [hp:0008988]
type: SIO_010056
comment: Phenotype [hp:0008988] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pelvic girdle muscle atrophy
in dataset: phenotype

Abnormal palmar dermatoglyphics [hp:0001018]
type: SIO_010056
comment: Phenotype [hp:0001018] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal palmar dermatoglyphics
in dataset: phenotype

Difficulty in tongue movements [hp:0000183]
type: SIO_010056
comment: Phenotype [hp:0000183] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Difficulty in tongue movements
in dataset: phenotype

Inflammatory arteriopathy [hp:0005291]
type: SIO_010056
comment: Phenotype [hp:0005291] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inflammatory arteriopathy
in dataset: phenotype

Perifollicular fibrosis [hp:0030054]
type: SIO_010056
comment: Phenotype [hp:0030054] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Perifollicular fibrosis
in dataset: phenotype

Clinodactyly of the 5th toe [hp:0001864]
type: SIO_010056
comment: Phenotype [hp:0001864] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Clinodactyly of the 5th toe
in dataset: phenotype

Streak ovary [hp:0010464]
type: SIO_010056
comment: Phenotype [hp:0010464] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Streak ovary
in dataset: phenotype

Interrupted aortic arch [hp:0011611]
type: SIO_010056
comment: Phenotype [hp:0011611] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Interrupted aortic arch
in dataset: phenotype

Atlantoaxial instability [hp:0003467]
type: SIO_010056
comment: Phenotype [hp:0003467] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atlantoaxial instability
in dataset: phenotype

Progressive macular scarring [hp:0007949]
type: SIO_010056
comment: Phenotype [hp:0007949] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive macular scarring
in dataset: phenotype

Episodic metabolic acidosis [hp:0004911]
type: SIO_010056
comment: Phenotype [hp:0004911] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic metabolic acidosis
in dataset: phenotype

Splayed epiphyses [hp:0200003]
type: SIO_010056
comment: Phenotype [hp:0200003] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Splayed epiphyses
in dataset: phenotype

Autoamputation of digits [hp:0007460]
type: SIO_010056
comment: Phenotype [hp:0007460] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autoamputation of digits
in dataset: phenotype

Chronic lymphatic leukemia [hp:0005550]
type: SIO_010056
comment: Phenotype [hp:0005550] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic lymphatic leukemia
in dataset: phenotype

Absence seizures [hp:0002121]
type: SIO_010056
comment: Phenotype [hp:0002121] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence seizures
in dataset: phenotype

Respiratory arrest [hp:0005943]
type: SIO_010056
comment: Phenotype [hp:0005943] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Respiratory arrest
in dataset: phenotype

Medial deviation of the foot [hp:0008082]
type: SIO_010056
comment: Phenotype [hp:0008082] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Medial deviation of the foot
in dataset: phenotype

Short palpebral fissure [hp:0012745]
type: SIO_010056
comment: Phenotype [hp:0012745] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short palpebral fissure
in dataset: phenotype

Widened posterior fossa [hp:0005445]
type: SIO_010056
comment: Phenotype [hp:0005445] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Widened posterior fossa
in dataset: phenotype

Hypergonadotropic hypogonadism [hp:0000815]
type: SIO_010056
comment: Phenotype [hp:0000815] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypergonadotropic hypogonadism
in dataset: phenotype

Abnormality of complement system [hp:0005339]
type: SIO_010056
comment: Phenotype [hp:0005339] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of complement system
in dataset: phenotype

Aseptic necrosis [hp:0010885]
type: SIO_010056
comment: Phenotype [hp:0010885] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aseptic necrosis
in dataset: phenotype

Visual field defect [hp:0001123]
type: SIO_010056
comment: Phenotype [hp:0001123] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Visual field defect
in dataset: phenotype

Prominent superficial veins [hp:0001015]
type: SIO_010056
comment: Phenotype [hp:0001015] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent superficial veins
in dataset: phenotype

Abnormal lower motor neuron morphology [hp:0002366]
type: SIO_010056
comment: Phenotype [hp:0002366] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal lower motor neuron morphology
in dataset: phenotype

Lobulated tongue [hp:0000180]
type: SIO_010056
comment: Phenotype [hp:0000180] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lobulated tongue
in dataset: phenotype

Superiorly displaced ears [hp:0008541]
type: SIO_010056
comment: Phenotype [hp:0008541] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Superiorly displaced ears
in dataset: phenotype

Thick nasal alae [hp:0009928]
type: SIO_010056
comment: Phenotype [hp:0009928] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thick nasal alae
in dataset: phenotype

Abnormality of the genital system [hp:0000078]
type: SIO_010056
comment: Phenotype [hp:0000078] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the genital system
in dataset: phenotype

Stiff skin [hp:0030053]
type: SIO_010056
comment: Phenotype [hp:0030053] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stiff skin
in dataset: phenotype

Aplasia of the ovary [hp:0010463]
type: SIO_010056
comment: Phenotype [hp:0010463] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the ovary
in dataset: phenotype

Short nail [hp:0001799]
type: SIO_010056
comment: Phenotype [hp:0001799] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short nail
in dataset: phenotype

Retinopathy [hp:0000488]
type: SIO_010056
comment: Phenotype [hp:0000488] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinopathy
in dataset: phenotype

Enlarged kidneys [hp:0000105]
type: SIO_010056
comment: Phenotype [hp:0000105] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged kidneys
in dataset: phenotype

Bicarbonate-wasting renal tubular acidosis [hp:0004910]
type: SIO_010056
comment: Phenotype [hp:0004910] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bicarbonate-wasting renal tubular acidosis
in dataset: phenotype

Enlarged metaphyses [hp:0003051]
type: SIO_010056
comment: Phenotype [hp:0003051] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged metaphyses
in dataset: phenotype

Dense posterior cortical cataract [hp:0007948]
type: SIO_010056
comment: Phenotype [hp:0007948] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dense posterior cortical cataract
in dataset: phenotype

Agnosia [hp:0010524]
type: SIO_010056
comment: Phenotype [hp:0010524] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Agnosia
in dataset: phenotype

Abnormality of the vertebrae [hp:0003468]
type: SIO_010056
comment: Phenotype [hp:0003468] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the vertebrae
in dataset: phenotype

Metacarpophalangeal joint contracture [hp:0006070]
type: SIO_010056
comment: Phenotype [hp:0006070] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metacarpophalangeal joint contracture
in dataset: phenotype

Loss of ability to walk in first decade [hp:0006794]
type: SIO_010056
comment: Phenotype [hp:0006794] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Loss of ability to walk in first decade
in dataset: phenotype

2nd-5th toe middle phalangeal hypoplasia [hp:0008083]
type: SIO_010056
comment: Phenotype [hp:0008083] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 2nd-5th toe middle phalangeal hypoplasia
in dataset: phenotype

Bacterial endocarditis [hp:0006689]
type: SIO_010056
comment: Phenotype [hp:0006689] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bacterial endocarditis
in dataset: phenotype

Cerebral cortical atrophy [hp:0002120]
type: SIO_010056
comment: Phenotype [hp:0002120] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral cortical atrophy
in dataset: phenotype

Sparse lateral eyebrow [hp:0005338]
type: SIO_010056
comment: Phenotype [hp:0005338] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sparse lateral eyebrow
in dataset: phenotype

Increased urinary cortisol level [hp:0012030]
type: SIO_010056
comment: Phenotype [hp:0012030] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased urinary cortisol level
in dataset: phenotype

Desquamative interstitial pneumonitis [hp:0005942]
type: SIO_010056
comment: Phenotype [hp:0005942] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Desquamative interstitial pneumonitis
in dataset: phenotype

Congenital nystagmus [hp:0006934]
type: SIO_010056
comment: Phenotype [hp:0006934] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital nystagmus
in dataset: phenotype

Gastrointestinal telangiectasia [hp:0002604]
type: SIO_010056
comment: Phenotype [hp:0002604] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gastrointestinal telangiectasia
in dataset: phenotype

Limb muscle weakness [hp:0003690]
type: SIO_010056
comment: Phenotype [hp:0003690] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb muscle weakness
in dataset: phenotype

Phalangeal dislocation [hp:0006243]
type: SIO_010056
comment: Phenotype [hp:0006243] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Phalangeal dislocation
in dataset: phenotype

Obtuse angle of mandible [hp:0005446]
type: SIO_010056
comment: Phenotype [hp:0005446] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Obtuse angle of mandible
in dataset: phenotype

Visual hallucinations [hp:0002367]
type: SIO_010056
comment: Phenotype [hp:0002367] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Visual hallucinations
in dataset: phenotype

Renal agenesis [hp:0000104]
type: SIO_010056
comment: Phenotype [hp:0000104] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal agenesis
in dataset: phenotype

Anonychia [hp:0001798]
type: SIO_010056
comment: Phenotype [hp:0001798] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anonychia
in dataset: phenotype

Inguinal freckling [hp:0030052]
type: SIO_010056
comment: Phenotype [hp:0030052] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inguinal freckling
in dataset: phenotype

Abnormality of the kidney [hp:0000077]
type: SIO_010056
comment: Phenotype [hp:0000077] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the kidney
in dataset: phenotype

Congenital strabismus [hp:0000487]
type: SIO_010056
comment: Phenotype [hp:0000487] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital strabismus
in dataset: phenotype

Increased intramuscular fat [hp:0008985]
type: SIO_010056
comment: Phenotype [hp:0008985] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased intramuscular fat
in dataset: phenotype

Broad metacarpals [hp:0001230]
type: SIO_010056
comment: Phenotype [hp:0001230] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad metacarpals
in dataset: phenotype

Strabismus [hp:0000486]
type: SIO_010056
comment: Phenotype [hp:0000486] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Strabismus
in dataset: phenotype

Gait apraxia [hp:0010521]
type: SIO_010056
comment: Phenotype [hp:0010521] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gait apraxia
in dataset: phenotype

Broad secondary alveolar ridge [hp:0000216]
type: SIO_010056
comment: Phenotype [hp:0000216] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad secondary alveolar ridge
in dataset: phenotype

Recurrent otitis media [hp:0000403]
type: SIO_010056
comment: Phenotype [hp:0000403] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent otitis media
in dataset: phenotype

Cystic liver disease [hp:0006706]
type: SIO_010056
comment: Phenotype [hp:0006706] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cystic liver disease
in dataset: phenotype

Long-chain dicarboxylic aciduria [hp:0008293]
type: SIO_010056
comment: Phenotype [hp:0008293] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long-chain dicarboxylic aciduria
in dataset: phenotype

Impaired distal tactile sensation [hp:0006937]
type: SIO_010056
comment: Phenotype [hp:0006937] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired distal tactile sensation
in dataset: phenotype

Abnormal echocardiogram [hp:0003116]
type: SIO_010056
comment: Phenotype [hp:0003116] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal echocardiogram
in dataset: phenotype

Precocious atherosclerosis [hp:0004416]
type: SIO_010056
comment: Phenotype [hp:0004416] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Precocious atherosclerosis
in dataset: phenotype

Hallux varus [hp:0008080]
type: SIO_010056
comment: Phenotype [hp:0008080] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hallux varus
in dataset: phenotype

Polyostotic fibrous dysplasia [hp:0010735]
type: SIO_010056
comment: Phenotype [hp:0010735] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polyostotic fibrous dysplasia
in dataset: phenotype

Radial deviation of thumb terminal phalanx [hp:0005895]
type: SIO_010056
comment: Phenotype [hp:0005895] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Radial deviation of thumb terminal phalanx
in dataset: phenotype

Excessive wrinkled skin [hp:0007392]
type: SIO_010056
comment: Phenotype [hp:0007392] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Excessive wrinkled skin
in dataset: phenotype

Metabolic alkalosis [hp:0200114]
type: SIO_010056
comment: Phenotype [hp:0200114] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metabolic alkalosis
in dataset: phenotype

Corneal scarring [hp:0000559]
type: SIO_010056
comment: Phenotype [hp:0000559] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corneal scarring
in dataset: phenotype

Amyotrophy of ankle musculature [hp:0009031]
type: SIO_010056
comment: Phenotype [hp:0009031] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Amyotrophy of ankle musculature
in dataset: phenotype

Abnormal form of the vertebral bodies [hp:0003312]
type: SIO_010056
comment: Phenotype [hp:0003312] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal form of the vertebral bodies
in dataset: phenotype

Dyslexia [hp:0010522]
type: SIO_010056
comment: Phenotype [hp:0010522] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dyslexia
in dataset: phenotype

Laryngeal cyst [hp:0100640]
type: SIO_010056
comment: Phenotype [hp:0100640] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laryngeal cyst
in dataset: phenotype

Megalocornea [hp:0000485]
type: SIO_010056
comment: Phenotype [hp:0000485] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Megalocornea
in dataset: phenotype

Thick upper lip vermilion [hp:0000215]
type: SIO_010056
comment: Phenotype [hp:0000215] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thick upper lip vermilion
in dataset: phenotype

Short stepped shuffling gait [hp:0007311]
type: SIO_010056
comment: Phenotype [hp:0007311] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short stepped shuffling gait
in dataset: phenotype

Loss of facial adipose tissue [hp:0000292]
type: SIO_010056
comment: Phenotype [hp:0000292] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Loss of facial adipose tissue
in dataset: phenotype

Progressive spastic quadriplegia [hp:0002478]
type: SIO_010056
comment: Phenotype [hp:0002478] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive spastic quadriplegia
in dataset: phenotype

Increased laxity of fingers [hp:0006149]
type: SIO_010056
comment: Phenotype [hp:0006149] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased laxity of fingers
in dataset: phenotype

Osteochondrosis dissecans [hp:0010886]
type: SIO_010056
comment: Phenotype [hp:0010886] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteochondrosis dissecans
in dataset: phenotype

Duodenal ulcer [hp:0002588]
type: SIO_010056
comment: Phenotype [hp:0002588] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Duodenal ulcer
in dataset: phenotype

Malignant mesothelioma [hp:0100001]
type: SIO_010056
comment: Phenotype [hp:0100001] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malignant mesothelioma
in dataset: phenotype

Abnormality of circulating hormone level [hp:0003117]
type: SIO_010056
comment: Phenotype [hp:0003117] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of circulating hormone level
in dataset: phenotype

Bilateral lung agenesis [hp:0005944]
type: SIO_010056
comment: Phenotype [hp:0005944] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral lung agenesis
in dataset: phenotype

Obliteration of the pulp chamber [hp:0006350]
type: SIO_010056
comment: Phenotype [hp:0006350] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Obliteration of the pulp chamber
in dataset: phenotype

Elfin facies [hp:0004428]
type: SIO_010056
comment: Phenotype [hp:0004428] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elfin facies
in dataset: phenotype

Abnormality of mitochondrial metabolism [hp:0003287]
type: SIO_010056
comment: Phenotype [hp:0003287] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of mitochondrial metabolism
in dataset: phenotype

Valgus foot deformity [hp:0008081]
type: SIO_010056
comment: Phenotype [hp:0008081] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Valgus foot deformity
in dataset: phenotype

Pulmonary artery stenosis [hp:0004415]
type: SIO_010056
comment: Phenotype [hp:0004415] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary artery stenosis
in dataset: phenotype

Pigment deposition in the trabecular meshwork [hp:0012631]
type: SIO_010056
comment: Phenotype [hp:0012631] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pigment deposition in the trabecular meshwork
in dataset: phenotype

Neuronal loss in the cerebral cortex [hp:0007190]
type: SIO_010056
comment: Phenotype [hp:0007190] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neuronal loss in the cerebral cortex
in dataset: phenotype

Aortic tortuosity [hp:0006687]
type: SIO_010056
comment: Phenotype [hp:0006687] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aortic tortuosity
in dataset: phenotype

Abnormality of the gastric mucosa [hp:0004295]
type: SIO_010056
comment: Phenotype [hp:0004295] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the gastric mucosa
in dataset: phenotype

Opacification of the corneal epithelium [hp:0007727]
type: SIO_010056
comment: Phenotype [hp:0007727] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Opacification of the corneal epithelium
in dataset: phenotype

Rieger anomaly [hp:0000558]
type: SIO_010056
comment: Phenotype [hp:0000558] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rieger anomaly
in dataset: phenotype

Scalp hair loss [hp:0200115]
type: SIO_010056
comment: Phenotype [hp:0200115] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scalp hair loss
in dataset: phenotype

Lip telangiectasia [hp:0000214]
type: SIO_010056
comment: Phenotype [hp:0000214] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lip telangiectasia
in dataset: phenotype

Hyperopic astigmatism [hp:0000484]
type: SIO_010056
comment: Phenotype [hp:0000484] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperopic astigmatism
in dataset: phenotype

Buphthalmos [hp:0000557]
type: SIO_010056
comment: Phenotype [hp:0000557] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Buphthalmos
in dataset: phenotype

Short chin [hp:0000331]
type: SIO_010056
comment: Phenotype [hp:0000331] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short chin
in dataset: phenotype

Neoplasm of the adrenal cortex [hp:0100641]
type: SIO_010056
comment: Phenotype [hp:0100641] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the adrenal cortex
in dataset: phenotype

Intimal thickening in the coronary arteries [hp:0005292]
type: SIO_010056
comment: Phenotype [hp:0005292] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intimal thickening in the coronary arteries
in dataset: phenotype

Impaired collagen-induced platelet aggregation [hp:0008320]
type: SIO_010056
comment: Phenotype [hp:0008320] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired collagen-induced platelet aggregation
in dataset: phenotype

Erythroderma [hp:0001019]
type: SIO_010056
comment: Phenotype [hp:0001019] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Erythroderma
in dataset: phenotype

Nail bed telangiectasia [hp:0001232]
type: SIO_010056
comment: Phenotype [hp:0001232] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nail bed telangiectasia
in dataset: phenotype

Myelomeningocele [hp:0002475]
type: SIO_010056
comment: Phenotype [hp:0002475] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myelomeningocele
in dataset: phenotype

Severe generalized osteoporosis [hp:0005897]
type: SIO_010056
comment: Phenotype [hp:0005897] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe generalized osteoporosis
in dataset: phenotype

Basal ganglia cysts [hp:0006799]
type: SIO_010056
comment: Phenotype [hp:0006799] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Basal ganglia cysts
in dataset: phenotype

Thrombophlebitis [hp:0004418]
type: SIO_010056
comment: Phenotype [hp:0004418] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thrombophlebitis
in dataset: phenotype

Hypoplasia of the tooth germ [hp:0006353]
type: SIO_010056
comment: Phenotype [hp:0006353] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the tooth germ
in dataset: phenotype

Abnormality of the odontoid process [hp:0003310]
type: SIO_010056
comment: Phenotype [hp:0003310] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the odontoid process
in dataset: phenotype

Decreased sensitivity to hypoxemia [hp:0005947]
type: SIO_010056
comment: Phenotype [hp:0005947] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased sensitivity to hypoxemia
in dataset: phenotype

Cystathioninemia [hp:0003286]
type: SIO_010056
comment: Phenotype [hp:0003286] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cystathioninemia
in dataset: phenotype

Aphalangy of the hands [hp:0005886]
type: SIO_010056
comment: Phenotype [hp:0005886] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aphalangy of the hands
in dataset: phenotype

Increased circulating cortisol level [hp:0003118]
type: SIO_010056
comment: Phenotype [hp:0003118] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased circulating cortisol level
in dataset: phenotype

Recurrent viral infections [hp:0004429]
type: SIO_010056
comment: Phenotype [hp:0004429] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent viral infections
in dataset: phenotype

Sclerotic cranial sutures [hp:0005441]
type: SIO_010056
comment: Phenotype [hp:0005441] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sclerotic cranial sutures
in dataset: phenotype

Conductive hearing impairment [hp:0000405]
type: SIO_010056
comment: Phenotype [hp:0000405] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Conductive hearing impairment
in dataset: phenotype

Cerebral degeneration [hp:0007313]
type: SIO_010056
comment: Phenotype [hp:0007313] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral degeneration
in dataset: phenotype

Venous insufficiency [hp:0005293]
type: SIO_010056
comment: Phenotype [hp:0005293] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Venous insufficiency
in dataset: phenotype

Retinal dystrophy [hp:0000556]
type: SIO_010056
comment: Phenotype [hp:0000556] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal dystrophy
in dataset: phenotype

Abnormality of the fingernails [hp:0001231]
type: SIO_010056
comment: Phenotype [hp:0001231] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the fingernails
in dataset: phenotype

Agenesis of the diaphragm [hp:0008986]
type: SIO_010056
comment: Phenotype [hp:0008986] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Agenesis of the diaphragm
in dataset: phenotype

Reduced factor X activity [hp:0008321]
type: SIO_010056
comment: Phenotype [hp:0008321] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced factor X activity
in dataset: phenotype

Astigmatism [hp:0000483]
type: SIO_010056
comment: Phenotype [hp:0000483] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Astigmatism
in dataset: phenotype

Aplasia/Hypoplasia of the nipples [hp:0006709]
type: SIO_010056
comment: Phenotype [hp:0006709] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the nipples
in dataset: phenotype

Irregular acetabular roof [hp:0008833]
type: SIO_010056
comment: Phenotype [hp:0008833] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular acetabular roof
in dataset: phenotype

Impaired vibration sensation at ankles [hp:0006938]
type: SIO_010056
comment: Phenotype [hp:0006938] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired vibration sensation at ankles
in dataset: phenotype

Abnormality of the forehead [hp:0000290]
type: SIO_010056
comment: Phenotype [hp:0000290] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the forehead
in dataset: phenotype

Primitive reflexes (palmomental, snout, glabellar) [hp:0002476]
type: SIO_010056
comment: Phenotype [hp:0002476] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Primitive reflexes (palmomental, snout, glabellar)
in dataset: phenotype

Intermittent claudication [hp:0004417]
type: SIO_010056
comment: Phenotype [hp:0004417] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intermittent claudication
in dataset: phenotype

Multicentric ossification of proximal femoral epiphyses [hp:0006450]
type: SIO_010056
comment: Phenotype [hp:0006450] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multicentric ossification of proximal femoral epiphyses
in dataset: phenotype

Ventilator dependence with inability to wean [hp:0005946]
type: SIO_010056
comment: Phenotype [hp:0005946] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ventilator dependence with inability to wean
in dataset: phenotype

Failure of eruption of permanent teeth [hp:0006352]
type: SIO_010056
comment: Phenotype [hp:0006352] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Failure of eruption of permanent teeth
in dataset: phenotype

Abnormality of lipid metabolism [hp:0003119]
type: SIO_010056
comment: Phenotype [hp:0003119] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of lipid metabolism
in dataset: phenotype

Widely patent coronal suture [hp:0005442]
type: SIO_010056
comment: Phenotype [hp:0005442] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Widely patent coronal suture
in dataset: phenotype

Hypoplasia of the odontoid process [hp:0003311]
type: SIO_010056
comment: Phenotype [hp:0003311] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the odontoid process
in dataset: phenotype

Arterial dissection [hp:0005294]
type: SIO_010056
comment: Phenotype [hp:0005294] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arterial dissection
in dataset: phenotype

Horner syndrome [hp:0002277]
type: SIO_010056
comment: Phenotype [hp:0002277] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Horner syndrome
in dataset: phenotype

Endocardial fibrosis [hp:0006685]
type: SIO_010056
comment: Phenotype [hp:0006685] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Endocardial fibrosis
in dataset: phenotype

Neoplasm of the central nervous system [hp:0100006]
type: SIO_010056
comment: Phenotype [hp:0100006] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the central nervous system
in dataset: phenotype

Triangular shaped proximal phalanx of the 3rd finger [hp:0009456]
type: SIO_010056
comment: Phenotype [hp:0009456] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular shaped proximal phalanx of the 3rd finger
in dataset: phenotype

Abnormality of the peritoneum [hp:0002585]
type: SIO_010056
comment: Phenotype [hp:0002585] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the peritoneum
in dataset: phenotype

Hitchhiker thumb [hp:0001234]
type: SIO_010056
comment: Phenotype [hp:0001234] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hitchhiker thumb
in dataset: phenotype

Abnormal mitochondrial morphology [hp:0008322]
type: SIO_010056
comment: Phenotype [hp:0008322] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal mitochondrial morphology
in dataset: phenotype

Yellow subcutaneous tissue covered by thin, scaly skin [hp:0007525]
type: SIO_010056
comment: Phenotype [hp:0007525] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Yellow subcutaneous tissue covered by thin, scaly skin
in dataset: phenotype

Doll-like facies [hp:0000295]
type: SIO_010056
comment: Phenotype [hp:0000295] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Doll-like facies
in dataset: phenotype

Microcornea [hp:0000482]
type: SIO_010056
comment: Phenotype [hp:0000482] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microcornea
in dataset: phenotype

Apneic episodes in infancy [hp:0005949]
type: SIO_010056
comment: Phenotype [hp:0005949] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Apneic episodes in infancy
in dataset: phenotype

Axillary apocrine gland hypoplasia [hp:0007397]
type: SIO_010056
comment: Phenotype [hp:0007397] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Axillary apocrine gland hypoplasia
in dataset: phenotype

Gingival overgrowth [hp:0000212]
type: SIO_010056
comment: Phenotype [hp:0000212] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gingival overgrowth
in dataset: phenotype

Immunodeficiency [hp:0002721]
type: SIO_010056
comment: Phenotype [hp:0002721] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Immunodeficiency
in dataset: phenotype

Abnormality of nail color [hp:0100643]
type: SIO_010056
comment: Phenotype [hp:0100643] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of nail color
in dataset: phenotype

Broad forehead [hp:0000337]
type: SIO_010056
comment: Phenotype [hp:0000337] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad forehead
in dataset: phenotype

Calf muscle hypertrophy [hp:0008981]
type: SIO_010056
comment: Phenotype [hp:0008981] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calf muscle hypertrophy
in dataset: phenotype

White matter neuronal heterotopia [hp:0007314]
type: SIO_010056
comment: Phenotype [hp:0007314] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: White matter neuronal heterotopia
in dataset: phenotype

Premature peripheral vascular disease [hp:0005299]
type: SIO_010056
comment: Phenotype [hp:0005299] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature peripheral vascular disease
in dataset: phenotype

Metacarpophalangeal synostosis [hp:0005880]
type: SIO_010056
comment: Phenotype [hp:0005880] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metacarpophalangeal synostosis
in dataset: phenotype

Ventricular preexcitation with multiple accessory pathways [hp:0006684]
type: SIO_010056
comment: Phenotype [hp:0006684] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ventricular preexcitation with multiple accessory pathways
in dataset: phenotype

Butterfly vertebrae [hp:0003316]
type: SIO_010056
comment: Phenotype [hp:0003316] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Butterfly vertebrae
in dataset: phenotype

Abnormality of the enteric ganglia [hp:0004362]
type: SIO_010056
comment: Phenotype [hp:0004362] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the enteric ganglia
in dataset: phenotype

Abnormal hair quantity [hp:0011362]
type: SIO_010056
comment: Phenotype [hp:0011362] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal hair quantity
in dataset: phenotype

Progressive forearm bowing [hp:0005891]
type: SIO_010056
comment: Phenotype [hp:0005891] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive forearm bowing
in dataset: phenotype

Generalized tonic-clonic seizures on awakening [hp:0007193]
type: SIO_010056
comment: Phenotype [hp:0007193] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized tonic-clonic seizures on awakening
in dataset: phenotype

Progressive ptosis [hp:0007838]
type: SIO_010056
comment: Phenotype [hp:0007838] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive ptosis
in dataset: phenotype

Cranium bifidum occultum [hp:0004423]
type: SIO_010056
comment: Phenotype [hp:0004423] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cranium bifidum occultum
in dataset: phenotype

Trichiasis [hp:0001128]
type: SIO_010056
comment: Phenotype [hp:0001128] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Trichiasis
in dataset: phenotype

Abnormal rod and cone electroretinograms [hp:0008323]
type: SIO_010056
comment: Phenotype [hp:0008323] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal rod and cone electroretinograms
in dataset: phenotype

Multicentric femoral head ossification [hp:0008835]
type: SIO_010056
comment: Phenotype [hp:0008835] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multicentric femoral head ossification
in dataset: phenotype

2-3 finger syndactyly [hp:0001233]
type: SIO_010056
comment: Phenotype [hp:0001233] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 2-3 finger syndactyly
in dataset: phenotype

Abnormality of the cornea [hp:0000481]
type: SIO_010056
comment: Phenotype [hp:0000481] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the cornea
in dataset: phenotype

Small nail [hp:0001792]
type: SIO_010056
comment: Phenotype [hp:0001792] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small nail
in dataset: phenotype

Trismus [hp:0000211]
type: SIO_010056
comment: Phenotype [hp:0000211] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Trismus
in dataset: phenotype

Microphallus [hp:0030260]
type: SIO_010056
comment: Phenotype [hp:0030260] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microphallus
in dataset: phenotype

Intestinal bleeding [hp:0002584]
type: SIO_010056
comment: Phenotype [hp:0002584] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intestinal bleeding
in dataset: phenotype

Prominent supraorbital ridges [hp:0000336]
type: SIO_010056
comment: Phenotype [hp:0000336] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent supraorbital ridges
in dataset: phenotype

IgA deficiency [hp:0002720]
type: SIO_010056
comment: Phenotype [hp:0002720] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: IgA deficiency
in dataset: phenotype

Abnormality of the left ventricle [hp:0001711]
type: SIO_010056
comment: Phenotype [hp:0001711] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the left ventricle
in dataset: phenotype

Macrotia [hp:0000400]
type: SIO_010056
comment: Phenotype [hp:0000400] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macrotia
in dataset: phenotype

Recurrent mandibular subluxations [hp:0005332]
type: SIO_010056
comment: Phenotype [hp:0005332] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent mandibular subluxations
in dataset: phenotype

Synovitis [hp:0100769]
type: SIO_010056
comment: Phenotype [hp:0100769] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Synovitis
in dataset: phenotype

Deviated nasal septum [hp:0004411]
type: SIO_010056
comment: Phenotype [hp:0004411] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deviated nasal septum
in dataset: phenotype

Adenomatous colonic polyposis [hp:0005227]
type: SIO_010056
comment: Phenotype [hp:0005227] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adenomatous colonic polyposis
in dataset: phenotype

Poor motor coordination [hp:0002275]
type: SIO_010056
comment: Phenotype [hp:0002275] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poor motor coordination
in dataset: phenotype

Hyporeflexia of upper limbs [hp:0012391]
type: SIO_010056
comment: Phenotype [hp:0012391] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyporeflexia of upper limbs
in dataset: phenotype

Aplasia/Hypoplasia of the phalanges of the toes [hp:0010173]
type: SIO_010056
comment: Phenotype [hp:0010173] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the phalanges of the toes
in dataset: phenotype

Retinal coloboma [hp:0000480]
type: SIO_010056
comment: Phenotype [hp:0000480] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal coloboma
in dataset: phenotype

Full cheeks [hp:0000293]
type: SIO_010056
comment: Phenotype [hp:0000293] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Full cheeks
in dataset: phenotype

Fetal ascites [hp:0001791]
type: SIO_010056
comment: Phenotype [hp:0001791] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fetal ascites
in dataset: phenotype

Projectile vomiting [hp:0002587]
type: SIO_010056
comment: Phenotype [hp:0002587] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Projectile vomiting
in dataset: phenotype

Ureterocele [hp:0000070]
type: SIO_010056
comment: Phenotype [hp:0000070] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ureterocele
in dataset: phenotype

Involuntary writhing movements [hp:0007316]
type: SIO_010056
comment: Phenotype [hp:0007316] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Involuntary writhing movements
in dataset: phenotype

Stippled calcification proximal humeral epiphyses [hp:0008838]
type: SIO_010056
comment: Phenotype [hp:0008838] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stippled calcification proximal humeral epiphyses
in dataset: phenotype

Schwannoma [hp:0100008]
type: SIO_010056
comment: Phenotype [hp:0100008] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Schwannoma
in dataset: phenotype

Left ventricular hypertrophy [hp:0001712]
type: SIO_010056
comment: Phenotype [hp:0001712] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Left ventricular hypertrophy
in dataset: phenotype

Cystocele [hp:0100645]
type: SIO_010056
comment: Phenotype [hp:0100645] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cystocele
in dataset: phenotype

Mosaic corneal dystrophy [hp:0007836]
type: SIO_010056
comment: Phenotype [hp:0007836] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mosaic corneal dystrophy
in dataset: phenotype

Endometriosis [hp:0030127]
type: SIO_010056
comment: Phenotype [hp:0030127] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Endometriosis
in dataset: phenotype

Dermatoglyphic variants [hp:0005882]
type: SIO_010056
comment: Phenotype [hp:0005882] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dermatoglyphic variants
in dataset: phenotype

Ventricular extrasystoles [hp:0006682]
type: SIO_010056
comment: Phenotype [hp:0006682] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ventricular extrasystoles
in dataset: phenotype

Prominent superficial blood vessels [hp:0007394]
type: SIO_010056
comment: Phenotype [hp:0007394] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent superficial blood vessels
in dataset: phenotype

Head-banging [hp:0012168]
type: SIO_010056
comment: Phenotype [hp:0012168] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Head-banging
in dataset: phenotype

Upbeat nystagmus [hp:0011477]
type: SIO_010056
comment: Phenotype [hp:0011477] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Upbeat nystagmus
in dataset: phenotype

Hand muscle atrophy [hp:0009130]
type: SIO_010056
comment: Phenotype [hp:0009130] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hand muscle atrophy
in dataset: phenotype

Flat forehead [hp:0004425]
type: SIO_010056
comment: Phenotype [hp:0004425] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flat forehead
in dataset: phenotype

Low alkaline phosphatase [hp:0003282]
type: SIO_010056
comment: Phenotype [hp:0003282] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low alkaline phosphatase
in dataset: phenotype

White hair [hp:0011364]
type: SIO_010056
comment: Phenotype [hp:0011364] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: White hair
in dataset: phenotype

Abnormality of the pulmonary artery [hp:0004414]
type: SIO_010056
comment: Phenotype [hp:0004414] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the pulmonary artery
in dataset: phenotype

Nonimmune hydrops fetalis [hp:0001790]
type: SIO_010056
comment: Phenotype [hp:0001790] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonimmune hydrops fetalis
in dataset: phenotype

Broad phalanx of the toes [hp:0010174]
type: SIO_010056
comment: Phenotype [hp:0010174] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad phalanx of the toes
in dataset: phenotype

Hypopigmented skin patches on arms [hp:0007526]
type: SIO_010056
comment: Phenotype [hp:0007526] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypopigmented skin patches on arms
in dataset: phenotype

Low anterior hairline [hp:0000294]
type: SIO_010056
comment: Phenotype [hp:0000294] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low anterior hairline
in dataset: phenotype

Peritonitis [hp:0002586]
type: SIO_010056
comment: Phenotype [hp:0002586] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peritonitis
in dataset: phenotype

Double eyebrow [hp:0010730]
type: SIO_010056
comment: Phenotype [hp:0010730] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Double eyebrow
in dataset: phenotype

Thyroiditis [hp:0100646]
type: SIO_010056
comment: Phenotype [hp:0100646] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thyroiditis
in dataset: phenotype

Stenosis of the external auditory canal [hp:0000402]
type: SIO_010056
comment: Phenotype [hp:0000402] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stenosis of the external auditory canal
in dataset: phenotype

Absent atrioventricular node [hp:0006681]
type: SIO_010056
comment: Phenotype [hp:0006681] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent atrioventricular node
in dataset: phenotype

Progressive gait ataxia [hp:0007240]
type: SIO_010056
comment: Phenotype [hp:0007240] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive gait ataxia
in dataset: phenotype

Hair-pulling [hp:0012167]
type: SIO_010056
comment: Phenotype [hp:0012167] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hair-pulling
in dataset: phenotype

Atrioventricular canal defect with right ventricle aorta and pulmonary atresia [hp:0005298]
type: SIO_010056
comment: Phenotype [hp:0005298] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atrioventricular canal defect with right ventricle aorta and pulmonary atresia
in dataset: phenotype

Increased serum ferritin [hp:0003281]
type: SIO_010056
comment: Phenotype [hp:0003281] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased serum ferritin
in dataset: phenotype

Tetraparesis [hp:0002273]
type: SIO_010056
comment: Phenotype [hp:0002273] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tetraparesis
in dataset: phenotype

Intestinal edema [hp:0005225]
type: SIO_010056
comment: Phenotype [hp:0005225] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intestinal edema
in dataset: phenotype

Profound sensorineural hearing impairment [hp:0011476]
type: SIO_010056
comment: Phenotype [hp:0011476] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Profound sensorineural hearing impairment
in dataset: phenotype

Urogenital sinus anomaly [hp:0100779]
type: SIO_010056
comment: Phenotype [hp:0100779] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urogenital sinus anomaly
in dataset: phenotype

Hemianopsia [hp:0012377]
type: SIO_010056
comment: Phenotype [hp:0012377] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemianopsia
in dataset: phenotype

Disc-like vertebral bodies [hp:0004591]
type: SIO_010056
comment: Phenotype [hp:0004591] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Disc-like vertebral bodies
in dataset: phenotype

Upper eyelid coloboma [hp:0000636]
type: SIO_010056
comment: Phenotype [hp:0000636] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Upper eyelid coloboma
in dataset: phenotype

Dilatation of the ascending aorta [hp:0005111]
type: SIO_010056
comment: Phenotype [hp:0005111] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dilatation of the ascending aorta
in dataset: phenotype

Elevated urine pyrophosphate [hp:0003491]
type: SIO_010056
comment: Phenotype [hp:0003491] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated urine pyrophosphate
in dataset: phenotype

Nonprogressive restrictive external ophthalmoplegia [hp:0007831]
type: SIO_010056
comment: Phenotype [hp:0007831] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonprogressive restrictive external ophthalmoplegia
in dataset: phenotype

Stomatocytosis [hp:0004446]
type: SIO_010056
comment: Phenotype [hp:0004446] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stomatocytosis
in dataset: phenotype

Pruritus [hp:0000989]
type: SIO_010056
comment: Phenotype [hp:0000989] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pruritus
in dataset: phenotype

Lethal skeletal dysplasia [hp:0005716]
type: SIO_010056
comment: Phenotype [hp:0005716] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lethal skeletal dysplasia
in dataset: phenotype

Urinary glycosaminoglycan excretion [hp:0003541]
type: SIO_010056
comment: Phenotype [hp:0003541] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urinary glycosaminoglycan excretion
in dataset: phenotype

Transient hyperlipidemia [hp:0008279]
type: SIO_010056
comment: Phenotype [hp:0008279] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Transient hyperlipidemia
in dataset: phenotype

Premature coronary artery disease [hp:0005181]
type: SIO_010056
comment: Phenotype [hp:0005181] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature coronary artery disease
in dataset: phenotype

Cholesteatoma [hp:0009797]
type: SIO_010056
comment: Phenotype [hp:0009797] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cholesteatoma
in dataset: phenotype

Aplasia/Hypoplasia of the middle phalanges of the toes [hp:0010194]
type: SIO_010056
comment: Phenotype [hp:0010194] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the middle phalanges of the toes
in dataset: phenotype

Anteverted ears [hp:0040080]
type: SIO_010056
comment: Phenotype [hp:0040080] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anteverted ears
in dataset: phenotype

Chronic atrophic gastritis [hp:0002582]
type: SIO_010056
comment: Phenotype [hp:0002582] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic atrophic gastritis
in dataset: phenotype

Hypoglycorrhachia [hp:0011972]
type: SIO_010056
comment: Phenotype [hp:0011972] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoglycorrhachia
in dataset: phenotype

Mask-like facies [hp:0000298]
type: SIO_010056
comment: Phenotype [hp:0000298] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mask-like facies
in dataset: phenotype

Commissural lip pit [hp:0002710]
type: SIO_010056
comment: Phenotype [hp:0002710] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Commissural lip pit
in dataset: phenotype

Long phalanx of finger [hp:0006155]
type: SIO_010056
comment: Phenotype [hp:0006155] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long phalanx of finger
in dataset: phenotype

Mixed hearing impairment [hp:0000410]
type: SIO_010056
comment: Phenotype [hp:0000410] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mixed hearing impairment
in dataset: phenotype

Abnormality of the epididymis [hp:0009714]
type: SIO_010056
comment: Phenotype [hp:0009714] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the epididymis
in dataset: phenotype

Loss of gluteal subcutaneous adipose tissue [hp:0009017]
type: SIO_010056
comment: Phenotype [hp:0009017] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Loss of gluteal subcutaneous adipose tissue
in dataset: phenotype

Agenesis of permanent teeth [hp:0006349]
type: SIO_010056
comment: Phenotype [hp:0006349] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Agenesis of permanent teeth
in dataset: phenotype

Abnormality of peripheral nerve conduction [hp:0003134]
type: SIO_010056
comment: Phenotype [hp:0003134] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of peripheral nerve conduction
in dataset: phenotype

Pigmentation of the sclera [hp:0007832]
type: SIO_010056
comment: Phenotype [hp:0007832] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pigmentation of the sclera
in dataset: phenotype

Hypoplastic sacrum [hp:0004590]
type: SIO_010056
comment: Phenotype [hp:0004590] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic sacrum
in dataset: phenotype

Blue irides [hp:0000635]
type: SIO_010056
comment: Phenotype [hp:0000635] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Blue irides
in dataset: phenotype

Lumbar hyperlordosis [hp:0002938]
type: SIO_010056
comment: Phenotype [hp:0002938] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lumbar hyperlordosis
in dataset: phenotype

Fatigue [hp:0012378]
type: SIO_010056
comment: Phenotype [hp:0012378] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fatigue
in dataset: phenotype

Flat cornea [hp:0007720]
type: SIO_010056
comment: Phenotype [hp:0007720] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flat cornea
in dataset: phenotype

High urinary gonadotropins (primary hypogonadism) [hp:0003492]
type: SIO_010056
comment: Phenotype [hp:0003492] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High urinary gonadotropins (primary hypogonadism)
in dataset: phenotype

Impaired platelet aggregation [hp:0003540]
type: SIO_010056
comment: Phenotype [hp:0003540] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired platelet aggregation
in dataset: phenotype

Atrial fibrillation [hp:0005110]
type: SIO_010056
comment: Phenotype [hp:0005110] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atrial fibrillation
in dataset: phenotype

Elliptocytosis [hp:0004445]
type: SIO_010056
comment: Phenotype [hp:0004445] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elliptocytosis
in dataset: phenotype

Skin rash [hp:0000988]
type: SIO_010056
comment: Phenotype [hp:0000988] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skin rash
in dataset: phenotype

Bicuspid pulmonary valve [hp:0005182]
type: SIO_010056
comment: Phenotype [hp:0005182] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bicuspid pulmonary valve
in dataset: phenotype

Bipartite calcaneus [hp:0008127]
type: SIO_010056
comment: Phenotype [hp:0008127] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bipartite calcaneus
in dataset: phenotype

Branchial cyst [hp:0009796]
type: SIO_010056
comment: Phenotype [hp:0009796] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Branchial cyst
in dataset: phenotype

Colitis [hp:0002583]
type: SIO_010056
comment: Phenotype [hp:0002583] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Colitis
in dataset: phenotype

Facial hypotonia [hp:0000297]
type: SIO_010056
comment: Phenotype [hp:0000297] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial hypotonia
in dataset: phenotype

Nail dystrophy [hp:0008404]
type: SIO_010056
comment: Phenotype [hp:0008404] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nail dystrophy
in dataset: phenotype

Dermatographic urticaria [hp:0011971]
type: SIO_010056
comment: Phenotype [hp:0011971] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dermatographic urticaria
in dataset: phenotype

Cryoglobulinemia [hp:0100778]
type: SIO_010056
comment: Phenotype [hp:0100778] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cryoglobulinemia
in dataset: phenotype

Papillary cystadenoma of the epididymis [hp:0009715]
type: SIO_010056
comment: Phenotype [hp:0009715] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Papillary cystadenoma of the epididymis
in dataset: phenotype

Absent eyelashes [hp:0000561]
type: SIO_010056
comment: Phenotype [hp:0000561] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent eyelashes
in dataset: phenotype

Abnormality of the spinocerebellar tracts [hp:0003133]
type: SIO_010056
comment: Phenotype [hp:0003133] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the spinocerebellar tracts
in dataset: phenotype

Anterior chamber synechiae [hp:0007833]
type: SIO_010056
comment: Phenotype [hp:0007833] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior chamber synechiae
in dataset: phenotype

Hemivertebrae [hp:0002937]
type: SIO_010056
comment: Phenotype [hp:0002937] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemivertebrae
in dataset: phenotype

Spherocytosis [hp:0004444]
type: SIO_010056
comment: Phenotype [hp:0004444] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spherocytosis
in dataset: phenotype

Decreased mean platelet volume [hp:0005537]
type: SIO_010056
comment: Phenotype [hp:0005537] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased mean platelet volume
in dataset: phenotype

Screwdriver-shaped incisors [hp:0006346]
type: SIO_010056
comment: Phenotype [hp:0006346] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Screwdriver-shaped incisors
in dataset: phenotype

EMG: axonal abnormality [hp:0003482]
type: SIO_010056
comment: Phenotype [hp:0003482] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EMG: axonal abnormality
in dataset: phenotype

Enlarged vertebral pedicles [hp:0004621]
type: SIO_010056
comment: Phenotype [hp:0004621] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged vertebral pedicles
in dataset: phenotype

Fused fourth and fifth metacarpals [hp:0005867]
type: SIO_010056
comment: Phenotype [hp:0005867] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fused fourth and fifth metacarpals
in dataset: phenotype

Oligodactyly [hp:0012165]
type: SIO_010056
comment: Phenotype [hp:0012165] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oligodactyly
in dataset: phenotype

Antinuclear antibody positivity [hp:0003493]
type: SIO_010056
comment: Phenotype [hp:0003493] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Antinuclear antibody positivity
in dataset: phenotype

Abnormality of mucopolysaccharide metabolism [hp:0011020]
type: SIO_010056
comment: Phenotype [hp:0011020] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of mucopolysaccharide metabolism
in dataset: phenotype

Talipes calcaneovarus [hp:0008124]
type: SIO_010056
comment: Phenotype [hp:0008124] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Talipes calcaneovarus
in dataset: phenotype

Branchial fistula [hp:0009795]
type: SIO_010056
comment: Phenotype [hp:0009795] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Branchial fistula
in dataset: phenotype

Happy demeanor [hp:0040082]
type: SIO_010056
comment: Phenotype [hp:0040082] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Happy demeanor
in dataset: phenotype

Abnormality of zinc homeostasis [hp:0008277]
type: SIO_010056
comment: Phenotype [hp:0008277] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of zinc homeostasis
in dataset: phenotype

Thoracolumbar interpediculate narrowness [hp:0008484]
type: SIO_010056
comment: Phenotype [hp:0008484] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thoracolumbar interpediculate narrowness
in dataset: phenotype

Small scrotum [hp:0030276]
type: SIO_010056
comment: Phenotype [hp:0030276] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small scrotum
in dataset: phenotype

Hypoplastic pelvis [hp:0008839]
type: SIO_010056
comment: Phenotype [hp:0008839] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic pelvis
in dataset: phenotype

Anterior hypopituitarism [hp:0000830]
type: SIO_010056
comment: Phenotype [hp:0000830] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior hypopituitarism
in dataset: phenotype

Y-linked inheritance [hp:0001450]
type: SIO_010056
comment: Phenotype [hp:0001450] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Y-linked inheritance
in dataset: phenotype

Decreased serum complement C9 [hp:0012308]
type: SIO_010056
comment: Phenotype [hp:0012308] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased serum complement C9
in dataset: phenotype

Right ventricular hypertrophy [hp:0001667]
type: SIO_010056
comment: Phenotype [hp:0001667] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Right ventricular hypertrophy
in dataset: phenotype

Diaminoaciduria [hp:0008339]
type: SIO_010056
comment: Phenotype [hp:0008339] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diaminoaciduria
in dataset: phenotype

Amegakaryocytic thrombocytopenia [hp:0004859]
type: SIO_010056
comment: Phenotype [hp:0004859] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Amegakaryocytic thrombocytopenia
in dataset: phenotype

Subependymal nodules [hp:0009716]
type: SIO_010056
comment: Phenotype [hp:0009716] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subependymal nodules
in dataset: phenotype

Exostoses [hp:0100777]
type: SIO_010056
comment: Phenotype [hp:0100777] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exostoses
in dataset: phenotype

Volvulus [hp:0002580]
type: SIO_010056
comment: Phenotype [hp:0002580] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Volvulus
in dataset: phenotype

Impaired ocular abduction [hp:0000634]
type: SIO_010056
comment: Phenotype [hp:0000634] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired ocular abduction
in dataset: phenotype

Nonprogressive cerebellar ataxia [hp:0002470]
type: SIO_010056
comment: Phenotype [hp:0002470] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonprogressive cerebellar ataxia
in dataset: phenotype

Myelofibrosis [hp:0011974]
type: SIO_010056
comment: Phenotype [hp:0011974] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myelofibrosis
in dataset: phenotype

Microdontia of primary teeth [hp:0006347]
type: SIO_010056
comment: Phenotype [hp:0006347] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microdontia of primary teeth
in dataset: phenotype

Progressive cataract [hp:0007834]
type: SIO_010056
comment: Phenotype [hp:0007834] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive cataract
in dataset: phenotype

Lambdoidal craniosynostosis [hp:0004443]
type: SIO_010056
comment: Phenotype [hp:0004443] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lambdoidal craniosynostosis
in dataset: phenotype

Distal sensory impairment [hp:0002936]
type: SIO_010056
comment: Phenotype [hp:0002936] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal sensory impairment
in dataset: phenotype

Increased serum pyruvate [hp:0003542]
type: SIO_010056
comment: Phenotype [hp:0003542] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased serum pyruvate
in dataset: phenotype

Metaphyseal enchondromatosis [hp:0005868]
type: SIO_010056
comment: Phenotype [hp:0005868] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metaphyseal enchondromatosis
in dataset: phenotype

Segmental peripheral demyelination/remyelination [hp:0003481]
type: SIO_010056
comment: Phenotype [hp:0003481] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Segmental peripheral demyelination/remyelination
in dataset: phenotype

Asymmetry of spinal facet joints [hp:0008482]
type: SIO_010056
comment: Phenotype [hp:0008482] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Asymmetry of spinal facet joints
in dataset: phenotype

Limited shoulder movement [hp:0006467]
type: SIO_010056
comment: Phenotype [hp:0006467] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited shoulder movement
in dataset: phenotype

Cerebellar cortical atrophy [hp:0008278]
type: SIO_010056
comment: Phenotype [hp:0008278] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebellar cortical atrophy
in dataset: phenotype

Branchial anomaly [hp:0009794]
type: SIO_010056
comment: Phenotype [hp:0009794] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Branchial anomaly
in dataset: phenotype

Second metatarsal posteriorly placed [hp:0008125]
type: SIO_010056
comment: Phenotype [hp:0008125] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Second metatarsal posteriorly placed
in dataset: phenotype

Tricuspid regurgitation [hp:0005180]
type: SIO_010056
comment: Phenotype [hp:0005180] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tricuspid regurgitation
in dataset: phenotype

Upper limb muscle hypoplasia [hp:0009016]
type: SIO_010056
comment: Phenotype [hp:0009016] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Upper limb muscle hypoplasia
in dataset: phenotype

Spatulate ribs [hp:0012307]
type: SIO_010056
comment: Phenotype [hp:0012307] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spatulate ribs
in dataset: phenotype

Keratoconus [hp:0000563]
type: SIO_010056
comment: Phenotype [hp:0000563] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Keratoconus
in dataset: phenotype

Recurrent pharyngitis [hp:0100776]
type: SIO_010056
comment: Phenotype [hp:0100776] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent pharyngitis
in dataset: phenotype

Cortical tubers [hp:0009717]
type: SIO_010056
comment: Phenotype [hp:0009717] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cortical tubers
in dataset: phenotype

Paroxysmal lethargy [hp:0011973]
type: SIO_010056
comment: Phenotype [hp:0011973] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paroxysmal lethargy
in dataset: phenotype

Decreased lacrimation [hp:0000633]
type: SIO_010056
comment: Phenotype [hp:0000633] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased lacrimation
in dataset: phenotype

Proximal symphalangism (hands) [hp:0006152]
type: SIO_010056
comment: Phenotype [hp:0006152] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal symphalangism (hands)
in dataset: phenotype

Dysplastic distal thumb phalanges with a central hole [hp:0005688]
type: SIO_010056
comment: Phenotype [hp:0005688] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysplastic distal thumb phalanges with a central hole
in dataset: phenotype

Ankle contracture [hp:0006466]
type: SIO_010056
comment: Phenotype [hp:0006466] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ankle contracture
in dataset: phenotype

Underdeveloped superior crus of antihelix [hp:0011246]
type: SIO_010056
comment: Phenotype [hp:0011246] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Underdeveloped superior crus of antihelix
in dataset: phenotype

Panhypogammaglobulinemia [hp:0003139]
type: SIO_010056
comment: Phenotype [hp:0003139] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Panhypogammaglobulinemia
in dataset: phenotype

Increased sensitivity to ionizing radiation [hp:0011133]
type: SIO_010056
comment: Phenotype [hp:0011133] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased sensitivity to ionizing radiation
in dataset: phenotype

Abnormality of primary molar morphology [hp:0006344]
type: SIO_010056
comment: Phenotype [hp:0006344] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of primary molar morphology
in dataset: phenotype

Hyperchromic macrocytic anemia [hp:0004857]
type: SIO_010056
comment: Phenotype [hp:0004857] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperchromic macrocytic anemia
in dataset: phenotype

Sagittal craniosynostosis [hp:0004442]
type: SIO_010056
comment: Phenotype [hp:0004442] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sagittal craniosynostosis
in dataset: phenotype

Supraventricular arrhythmia [hp:0005115]
type: SIO_010056
comment: Phenotype [hp:0005115] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Supraventricular arrhythmia
in dataset: phenotype

Downturned corners of mouth [hp:0002714]
type: SIO_010056
comment: Phenotype [hp:0002714] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Downturned corners of mouth
in dataset: phenotype

Hip dislocation [hp:0002827]
type: SIO_010056
comment: Phenotype [hp:0002827] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hip dislocation
in dataset: phenotype

Chin with horizontal crease [hp:0011823]
type: SIO_010056
comment: Phenotype [hp:0011823] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chin with horizontal crease
in dataset: phenotype

Lacrimation abnormality [hp:0000632]
type: SIO_010056
comment: Phenotype [hp:0000632] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lacrimation abnormality
in dataset: phenotype

Hypoglycemia [hp:0001943]
type: SIO_010056
comment: Phenotype [hp:0001943] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoglycemia
in dataset: phenotype

Hyperreflexia [hp:0001347]
type: SIO_010056
comment: Phenotype [hp:0001347] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperreflexia
in dataset: phenotype

Small cerebral cortex [hp:0002472]
type: SIO_010056
comment: Phenotype [hp:0002472] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small cerebral cortex
in dataset: phenotype

Autosomal dominant contiguous gene syndrome [hp:0001452]
type: SIO_010056
comment: Phenotype [hp:0001452] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autosomal dominant contiguous gene syndrome
in dataset: phenotype

Dural ectasia [hp:0100775]
type: SIO_010056
comment: Phenotype [hp:0100775] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dural ectasia
in dataset: phenotype

Lacrimal duct atresia [hp:0000564]
type: SIO_010056
comment: Phenotype [hp:0000564] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lacrimal duct atresia
in dataset: phenotype

Mesoaxial hand polydactyly [hp:0006159]
type: SIO_010056
comment: Phenotype [hp:0006159] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mesoaxial hand polydactyly
in dataset: phenotype

Pursed lips [hp:0000205]
type: SIO_010056
comment: Phenotype [hp:0000205] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pursed lips
in dataset: phenotype

Spinocerebellar tract degeneration [hp:0002503]
type: SIO_010056
comment: Phenotype [hp:0002503] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinocerebellar tract degeneration
in dataset: phenotype

Abnormal cone-mediated electroretinogram [hp:0008275]
type: SIO_010056
comment: Phenotype [hp:0008275] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal cone-mediated electroretinogram
in dataset: phenotype

Nephrogenic rest [hp:0100880]
type: SIO_010056
comment: Phenotype [hp:0100880] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nephrogenic rest
in dataset: phenotype

Absent smooth pursuit [hp:0007179]
type: SIO_010056
comment: Phenotype [hp:0007179] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent smooth pursuit
in dataset: phenotype

Periosteal thickening of long tubular bones [hp:0006465]
type: SIO_010056
comment: Phenotype [hp:0006465] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Periosteal thickening of long tubular bones
in dataset: phenotype

Opposable triphalangeal thumb [hp:0005866]
type: SIO_010056
comment: Phenotype [hp:0005866] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Opposable triphalangeal thumb
in dataset: phenotype

Cervical spondylosis [hp:0008480]
type: SIO_010056
comment: Phenotype [hp:0008480] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cervical spondylosis
in dataset: phenotype

Increased blood urea nitrogen (BUN) [hp:0003138]
type: SIO_010056
comment: Phenotype [hp:0003138] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased blood urea nitrogen (BUN)
in dataset: phenotype

Hump-shaped mound of bone in central and posterior portions of vertebral endplate [hp:0004594]
type: SIO_010056
comment: Phenotype [hp:0004594] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hump-shaped mound of bone in central and posterior portions of vertebral endplate
in dataset: phenotype

Dumbbell-shaped humerus [hp:0005009]
type: SIO_010056
comment: Phenotype [hp:0005009] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dumbbell-shaped humerus
in dataset: phenotype

Hypoplasia of the corpus callosum [hp:0002079]
type: SIO_010056
comment: Phenotype [hp:0002079] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the corpus callosum
in dataset: phenotype

Glossitis [hp:0000206]
type: SIO_010056
comment: Phenotype [hp:0000206] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glossitis
in dataset: phenotype

Multiple joint contractures [hp:0002828]
type: SIO_010056
comment: Phenotype [hp:0002828] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple joint contractures
in dataset: phenotype

Broad chin [hp:0011822]
type: SIO_010056
comment: Phenotype [hp:0011822] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad chin
in dataset: phenotype

Abnormality of the immune system [hp:0002715]
type: SIO_010056
comment: Phenotype [hp:0002715] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the immune system
in dataset: phenotype

Hyperostosis [hp:0100774]
type: SIO_010056
comment: Phenotype [hp:0100774] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperostosis
in dataset: phenotype

Bradycardia [hp:0001662]
type: SIO_010056
comment: Phenotype [hp:0001662] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bradycardia
in dataset: phenotype

Metabolic acidosis [hp:0001942]
type: SIO_010056
comment: Phenotype [hp:0001942] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metabolic acidosis
in dataset: phenotype

Esotropia [hp:0000565]
type: SIO_010056
comment: Phenotype [hp:0000565] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Esotropia
in dataset: phenotype

Hypomelanotic macules [hp:0009719]
type: SIO_010056
comment: Phenotype [hp:0009719] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypomelanotic macules
in dataset: phenotype

Early onset of sexual maturation [hp:0100000]
type: SIO_010056
comment: Phenotype [hp:0100000] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Early onset of sexual maturation
in dataset: phenotype

Finger joint hyperextensibility [hp:0006158]
type: SIO_010056
comment: Phenotype [hp:0006158] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Finger joint hyperextensibility
in dataset: phenotype

Cutaneous amyloidosis [hp:0012309]
type: SIO_010056
comment: Phenotype [hp:0012309] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cutaneous amyloidosis
in dataset: phenotype

Motor polyneuropathy [hp:0007178]
type: SIO_010056
comment: Phenotype [hp:0007178] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Motor polyneuropathy
in dataset: phenotype

Onycholysis of distal fingernails [hp:0008400]
type: SIO_010056
comment: Phenotype [hp:0008400] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Onycholysis of distal fingernails
in dataset: phenotype

Toe walking [hp:0040083]
type: SIO_010056
comment: Phenotype [hp:0040083] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Toe walking
in dataset: phenotype

Prolinuria [hp:0003137]
type: SIO_010056
comment: Phenotype [hp:0003137] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolinuria
in dataset: phenotype

Peg-shaped maxillary lateral incisors [hp:0006342]
type: SIO_010056
comment: Phenotype [hp:0006342] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peg-shaped maxillary lateral incisors
in dataset: phenotype

Type E brachydactyly [hp:0005863]
type: SIO_010056
comment: Phenotype [hp:0005863] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type E brachydactyly
in dataset: phenotype

Dilatation of the aortic arch [hp:0005113]
type: SIO_010056
comment: Phenotype [hp:0005113] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dilatation of the aortic arch
in dataset: phenotype

Lymphadenopathy [hp:0002716]
type: SIO_010056
comment: Phenotype [hp:0002716] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lymphadenopathy
in dataset: phenotype

Shoulder girdle muscle weakness [hp:0003547]
type: SIO_010056
comment: Phenotype [hp:0003547] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shoulder girdle muscle weakness
in dataset: phenotype

Large joint dislocations [hp:0005008]
type: SIO_010056
comment: Phenotype [hp:0005008] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large joint dislocations
in dataset: phenotype

Patchy osteosclerosis [hp:0005686]
type: SIO_010056
comment: Phenotype [hp:0005686] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Patchy osteosclerosis
in dataset: phenotype

Increased serum beta-hexosaminidase [hp:0003333]
type: SIO_010056
comment: Phenotype [hp:0003333] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased serum beta-hexosaminidase
in dataset: phenotype

Abnormality of the gastrointestinal tract [hp:0011024]
type: SIO_010056
comment: Phenotype [hp:0011024] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the gastrointestinal tract
in dataset: phenotype

Arthralgia [hp:0002829]
type: SIO_010056
comment: Phenotype [hp:0002829] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arthralgia
in dataset: phenotype

Triangular mouth [hp:0000207]
type: SIO_010056
comment: Phenotype [hp:0000207] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular mouth
in dataset: phenotype

Reduced protein S activity [hp:0004855]
type: SIO_010056
comment: Phenotype [hp:0004855] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced protein S activity
in dataset: phenotype

Coronal craniosynostosis [hp:0004440]
type: SIO_010056
comment: Phenotype [hp:0004440] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coronal craniosynostosis
in dataset: phenotype

Neoplasm of the endocrine system [hp:0100568]
type: SIO_010056
comment: Phenotype [hp:0100568] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the endocrine system
in dataset: phenotype

Cerebral amyloid angiopathy [hp:0011970]
type: SIO_010056
comment: Phenotype [hp:0011970] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral amyloid angiopathy
in dataset: phenotype

Expressive language delay [hp:0002474]
type: SIO_010056
comment: Phenotype [hp:0002474] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Expressive language delay
in dataset: phenotype

Acidosis [hp:0001941]
type: SIO_010056
comment: Phenotype [hp:0001941] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acidosis
in dataset: phenotype

Facial diplegia [hp:0001349]
type: SIO_010056
comment: Phenotype [hp:0001349] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial diplegia
in dataset: phenotype

Ventricular fibrillation [hp:0001663]
type: SIO_010056
comment: Phenotype [hp:0001663] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ventricular fibrillation
in dataset: phenotype

Cartilage destruction [hp:0100773]
type: SIO_010056
comment: Phenotype [hp:0100773] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cartilage destruction
in dataset: phenotype

Onychogryposis of toenails [hp:0008401]
type: SIO_010056
comment: Phenotype [hp:0008401] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Onychogryposis of toenails
in dataset: phenotype

Antegonial notching of mandible [hp:0003779]
type: SIO_010056
comment: Phenotype [hp:0003779] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Antegonial notching of mandible
in dataset: phenotype

Neonatal death [hp:0003811]
type: SIO_010056
comment: Phenotype [hp:0003811] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neonatal death
in dataset: phenotype

Spasticity of pharyngeal muscles [hp:0002501]
type: SIO_010056
comment: Phenotype [hp:0002501] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spasticity of pharyngeal muscles
in dataset: phenotype

Pseudobulbar paralysis [hp:0007024]
type: SIO_010056
comment: Phenotype [hp:0007024] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pseudobulbar paralysis
in dataset: phenotype

Adult-onset night blindness [hp:0007830]
type: SIO_010056
comment: Phenotype [hp:0007830] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adult-onset night blindness
in dataset: phenotype

Chronic furunculosis [hp:0011132]
type: SIO_010056
comment: Phenotype [hp:0011132] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic furunculosis
in dataset: phenotype

Metaphyseal dysostosis [hp:0005899]
type: SIO_010056
comment: Phenotype [hp:0005899] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metaphyseal dysostosis
in dataset: phenotype

Osteopoikilosis [hp:0010739]
type: SIO_010056
comment: Phenotype [hp:0010739] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteopoikilosis
in dataset: phenotype

Chronic kidney disease [hp:0012622]
type: SIO_010056
comment: Phenotype [hp:0012622] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic kidney disease
in dataset: phenotype

Transient aminoaciduria [hp:0008273]
type: SIO_010056
comment: Phenotype [hp:0008273] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Transient aminoaciduria
in dataset: phenotype

Pseudoarthrosis [hp:0005864]
type: SIO_010056
comment: Phenotype [hp:0005864] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pseudoarthrosis
in dataset: phenotype

Defective dehydrogenation of isovaleryl CoA and butyryl CoA [hp:0003490]
type: SIO_010056
comment: Phenotype [hp:0003490] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Defective dehydrogenation of isovaleryl CoA and butyryl CoA
in dataset: phenotype

Absent primary metaphyseal spongiosa [hp:0003332]
type: SIO_010056
comment: Phenotype [hp:0003332] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent primary metaphyseal spongiosa
in dataset: phenotype

Abnormality of cardiovascular system physiology [hp:0011025]
type: SIO_010056
comment: Phenotype [hp:0011025] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of cardiovascular system physiology
in dataset: phenotype

Microphakia [hp:0012376]
type: SIO_010056
comment: Phenotype [hp:0012376] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microphakia
in dataset: phenotype

Thoracic platyspondyly [hp:0004592]
type: SIO_010056
comment: Phenotype [hp:0004592] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thoracic platyspondyly
in dataset: phenotype

Chin with H-shaped crease [hp:0011824]
type: SIO_010056
comment: Phenotype [hp:0011824] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chin with H-shaped crease
in dataset: phenotype

Loss of retinal pigment epithelium [hp:0007722]
type: SIO_010056
comment: Phenotype [hp:0007722] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Loss of retinal pigment epithelium
in dataset: phenotype

Exercise intolerance [hp:0003546]
type: SIO_010056
comment: Phenotype [hp:0003546] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exercise intolerance
in dataset: phenotype

Hypoplasia of serratus anterior muscle [hp:0009011]
type: SIO_010056
comment: Phenotype [hp:0009011] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of serratus anterior muscle
in dataset: phenotype

Erectile abnormalities [hp:0100639]
type: SIO_010056
comment: Phenotype [hp:0100639] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Erectile abnormalities
in dataset: phenotype

Normochromic microcytic anemia [hp:0004856]
type: SIO_010056
comment: Phenotype [hp:0004856] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Normochromic microcytic anemia
in dataset: phenotype

Abnormal vertebral ossification [hp:0100569]
type: SIO_010056
comment: Phenotype [hp:0100569] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal vertebral ossification
in dataset: phenotype

Chorioretinal coloboma [hp:0000567]
type: SIO_010056
comment: Phenotype [hp:0000567] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chorioretinal coloboma
in dataset: phenotype

Abnormality of the umbilicus [hp:0001551]
type: SIO_010056
comment: Phenotype [hp:0001551] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the umbilicus
in dataset: phenotype

Torsade de pointes [hp:0001664]
type: SIO_010056
comment: Phenotype [hp:0001664] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Torsade de pointes
in dataset: phenotype

Brisk reflexes [hp:0001348]
type: SIO_010056
comment: Phenotype [hp:0001348] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Brisk reflexes
in dataset: phenotype

Phenotypic variability [hp:0003812]
type: SIO_010056
comment: Phenotype [hp:0003812] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Phenotypic variability
in dataset: phenotype

Abnormality of the cerebral white matter [hp:0002500]
type: SIO_010056
comment: Phenotype [hp:0002500] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the cerebral white matter
in dataset: phenotype

Ridged fingernail [hp:0008402]
type: SIO_010056
comment: Phenotype [hp:0008402] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ridged fingernail
in dataset: phenotype

Short mandibular rami [hp:0003778]
type: SIO_010056
comment: Phenotype [hp:0003778] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short mandibular rami
in dataset: phenotype

Antenatal intracerebral hemorrhage [hp:0007023]
type: SIO_010056
comment: Phenotype [hp:0007023] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Antenatal intracerebral hemorrhage
in dataset: phenotype

Euthyroid goiter [hp:0009798]
type: SIO_010056
comment: Phenotype [hp:0009798] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Euthyroid goiter
in dataset: phenotype

Congenital hepatic fibrosis [hp:0002612]
type: SIO_010056
comment: Phenotype [hp:0002612] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital hepatic fibrosis
in dataset: phenotype

Cutaneous photosensitivity [hp:0000992]
type: SIO_010056
comment: Phenotype [hp:0000992] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cutaneous photosensitivity
in dataset: phenotype

Pili torti [hp:0003777]
type: SIO_010056
comment: Phenotype [hp:0003777] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pili torti
in dataset: phenotype

Abnormality of the femur [hp:0002823]
type: SIO_010056
comment: Phenotype [hp:0002823] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the femur
in dataset: phenotype

Hypoperistalsis [hp:0100771]
type: SIO_010056
comment: Phenotype [hp:0100771] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoperistalsis
in dataset: phenotype

Barrel-shaped chest [hp:0001552]
type: SIO_010056
comment: Phenotype [hp:0001552] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Barrel-shaped chest
in dataset: phenotype

Orthostatic hypotension due to autonomic dysfunction [hp:0004926]
type: SIO_010056
comment: Phenotype [hp:0004926] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Orthostatic hypotension due to autonomic dysfunction
in dataset: phenotype

Ivory epiphyses of the distal phalanges of the hand [hp:0010252]
type: SIO_010056
comment: Phenotype [hp:0010252] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ivory epiphyses of the distal phalanges of the hand
in dataset: phenotype

Absent hand [hp:0004050]
type: SIO_010056
comment: Phenotype [hp:0004050] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent hand
in dataset: phenotype

Kernicterus [hp:0001343]
type: SIO_010056
comment: Phenotype [hp:0001343] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Kernicterus
in dataset: phenotype

Abnormality of brainstem morphology [hp:0002363]
type: SIO_010056
comment: Phenotype [hp:0002363] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of brainstem morphology
in dataset: phenotype

Abnormality of neutrophils [hp:0001874]
type: SIO_010056
comment: Phenotype [hp:0001874] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of neutrophils
in dataset: phenotype

Recurrent bacterial infections [hp:0002718]
type: SIO_010056
comment: Phenotype [hp:0002718] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent bacterial infections
in dataset: phenotype

Renal tubular acidosis [hp:0001947]
type: SIO_010056
comment: Phenotype [hp:0001947] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal tubular acidosis
in dataset: phenotype

Abnormality of connective tissue [hp:0003549]
type: SIO_010056
comment: Phenotype [hp:0003549] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of connective tissue
in dataset: phenotype

Distal arthrogryposis [hp:0005684]
type: SIO_010056
comment: Phenotype [hp:0005684] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal arthrogryposis
in dataset: phenotype

Decreased osteoclast count [hp:0030328]
type: SIO_010056
comment: Phenotype [hp:0030328] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased osteoclast count
in dataset: phenotype

Scapuloperoneal weakness [hp:0003704]
type: SIO_010056
comment: Phenotype [hp:0003704] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scapuloperoneal weakness
in dataset: phenotype

Cerebral vasculitis [hp:0005318]
type: SIO_010056
comment: Phenotype [hp:0005318] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral vasculitis
in dataset: phenotype

Intrahepatic cholestasis with episodic jaundice [hp:0006575]
type: SIO_010056
comment: Phenotype [hp:0006575] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intrahepatic cholestasis with episodic jaundice
in dataset: phenotype

Absent or minimally ossified vertebral bodies [hp:0004599]
type: SIO_010056
comment: Phenotype [hp:0004599] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent or minimally ossified vertebral bodies
in dataset: phenotype

Hyperthyroidism [hp:0000836]
type: SIO_010056
comment: Phenotype [hp:0000836] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperthyroidism
in dataset: phenotype

Migraine [hp:0002076]
type: SIO_010056
comment: Phenotype [hp:0002076] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Migraine
in dataset: phenotype

Pain insensitivity [hp:0007021]
type: SIO_010056
comment: Phenotype [hp:0007021] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pain insensitivity
in dataset: phenotype

Molluscoid pseudotumors [hp:0000993]
type: SIO_010056
comment: Phenotype [hp:0000993] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Molluscoid pseudotumors
in dataset: phenotype

Abnormal foot bone ossification [hp:0010675]
type: SIO_010056
comment: Phenotype [hp:0010675] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal foot bone ossification
in dataset: phenotype

Cholestatic liver disease [hp:0002611]
type: SIO_010056
comment: Phenotype [hp:0002611] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cholestatic liver disease
in dataset: phenotype

Pallor [hp:0000980]
type: SIO_010056
comment: Phenotype [hp:0000980] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pallor
in dataset: phenotype

Hyperperistalsis [hp:0100770]
type: SIO_010056
comment: Phenotype [hp:0100770] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperperistalsis
in dataset: phenotype

Patent urachus [hp:0010479]
type: SIO_010056
comment: Phenotype [hp:0010479] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Patent urachus
in dataset: phenotype

Thrombocytopenia [hp:0001873]
type: SIO_010056
comment: Phenotype [hp:0001873] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thrombocytopenia
in dataset: phenotype

Pulmonary artery dilatation [hp:0004927]
type: SIO_010056
comment: Phenotype [hp:0004927] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary artery dilatation
in dataset: phenotype

Aplasia/Hypoplasia involving the nose [hp:0009924]
type: SIO_010056
comment: Phenotype [hp:0009924] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia involving the nose
in dataset: phenotype

Thyroid hormone receptor defect [hp:0002930]
type: SIO_010056
comment: Phenotype [hp:0002930] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thyroid hormone receptor defect
in dataset: phenotype

Shuffling gait [hp:0002362]
type: SIO_010056
comment: Phenotype [hp:0002362] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shuffling gait
in dataset: phenotype

Cerebral hemorrhage [hp:0001342]
type: SIO_010056
comment: Phenotype [hp:0001342] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral hemorrhage
in dataset: phenotype

Hypoxemia [hp:0012418]
type: SIO_010056
comment: Phenotype [hp:0012418] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoxemia
in dataset: phenotype

Steatocystoma multiplex [hp:0012035]
type: SIO_010056
comment: Phenotype [hp:0012035] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Steatocystoma multiplex
in dataset: phenotype

Recurrent infections [hp:0002719]
type: SIO_010056
comment: Phenotype [hp:0002719] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent infections
in dataset: phenotype

Babinski sign [hp:0003487]
type: SIO_010056
comment: Phenotype [hp:0003487] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Babinski sign
in dataset: phenotype

Subsarcolemmal accumulations of abnormally shaped mitochondria [hp:0003548]
type: SIO_010056
comment: Phenotype [hp:0003548] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subsarcolemmal accumulations of abnormally shaped mitochondria
in dataset: phenotype

Elevated urinary dopamine [hp:0011979]
type: SIO_010056
comment: Phenotype [hp:0011979] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated urinary dopamine
in dataset: phenotype

Intermittent thrombocytopenia [hp:0004854]
type: SIO_010056
comment: Phenotype [hp:0004854] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intermittent thrombocytopenia
in dataset: phenotype

Femoral bowing present at birth, straightening with time [hp:0005005]
type: SIO_010056
comment: Phenotype [hp:0005005] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Femoral bowing present at birth, straightening with time
in dataset: phenotype

Ketosis [hp:0001946]
type: SIO_010056
comment: Phenotype [hp:0001946] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ketosis
in dataset: phenotype

Hepatic arteriovenous malformation [hp:0006574]
type: SIO_010056
comment: Phenotype [hp:0006574] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatic arteriovenous malformation
in dataset: phenotype

Adrenal hypoplasia [hp:0000835]
type: SIO_010056
comment: Phenotype [hp:0000835] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenal hypoplasia
in dataset: phenotype

Dysdiadochokinesis [hp:0002075]
type: SIO_010056
comment: Phenotype [hp:0002075] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysdiadochokinesis
in dataset: phenotype

Slender metacarpals [hp:0006236]
type: SIO_010056
comment: Phenotype [hp:0006236] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slender metacarpals
in dataset: phenotype

Supernumerary vertebral ossification centers [hp:0004598]
type: SIO_010056
comment: Phenotype [hp:0004598] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Supernumerary vertebral ossification centers
in dataset: phenotype

Progressive spastic paraplegia [hp:0007020]
type: SIO_010056
comment: Phenotype [hp:0007020] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive spastic paraplegia
in dataset: phenotype

Small cervical vertebral bodies [hp:0004629]
type: SIO_010056
comment: Phenotype [hp:0004629] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small cervical vertebral bodies
in dataset: phenotype

Broad distal phalanx of the thumb [hp:0009642]
type: SIO_010056
comment: Phenotype [hp:0009642] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad distal phalanx of the thumb
in dataset: phenotype

Hypoplasia of the brainstem [hp:0002365]
type: SIO_010056
comment: Phenotype [hp:0002365] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the brainstem
in dataset: phenotype

Aplasia of the nose [hp:0009927]
type: SIO_010056
comment: Phenotype [hp:0009927] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the nose
in dataset: phenotype

Abnormality of the urinary system [hp:0000079]
type: SIO_010056
comment: Phenotype [hp:0000079] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the urinary system
in dataset: phenotype

Psychotic mentation [hp:0001345]
type: SIO_010056
comment: Phenotype [hp:0001345] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Psychotic mentation
in dataset: phenotype

Abnormality of thrombocytes [hp:0001872]
type: SIO_010056
comment: Phenotype [hp:0001872] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of thrombocytes
in dataset: phenotype

Ureteral obstruction [hp:0006000]
type: SIO_010056
comment: Phenotype [hp:0006000] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ureteral obstruction
in dataset: phenotype

Abnormal oral glucose tolerance [hp:0004924]
type: SIO_010056
comment: Phenotype [hp:0004924] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal oral glucose tolerance
in dataset: phenotype

Elevated diastolic blood pressure [hp:0005117]
type: SIO_010056
comment: Phenotype [hp:0005117] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated diastolic blood pressure
in dataset: phenotype

Folate-responsive megaloblastic anemia [hp:0004851]
type: SIO_010056
comment: Phenotype [hp:0004851] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Folate-responsive megaloblastic anemia
in dataset: phenotype

Fever [hp:0001945]
type: SIO_010056
comment: Phenotype [hp:0001945] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fever
in dataset: phenotype

Caudal appendage [hp:0002825]
type: SIO_010056
comment: Phenotype [hp:0002825] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Caudal appendage
in dataset: phenotype

Sternocleidomastoid amyotrophy [hp:0012036]
type: SIO_010056
comment: Phenotype [hp:0012036] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sternocleidomastoid amyotrophy
in dataset: phenotype

Polymicrogyria [hp:0002126]
type: SIO_010056
comment: Phenotype [hp:0002126] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polymicrogyria
in dataset: phenotype

Malaligned carpal bone [hp:0006092]
type: SIO_010056
comment: Phenotype [hp:0006092] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malaligned carpal bone
in dataset: phenotype

Acute hepatic steatosis [hp:0006573]
type: SIO_010056
comment: Phenotype [hp:0006573] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute hepatic steatosis
in dataset: phenotype

Truncal ataxia [hp:0002078]
type: SIO_010056
comment: Phenotype [hp:0002078] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Truncal ataxia
in dataset: phenotype

Lower limb pain [hp:0012514]
type: SIO_010056
comment: Phenotype [hp:0012514] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lower limb pain
in dataset: phenotype

Decreased muscle glycogen content [hp:0012270]
type: SIO_010056
comment: Phenotype [hp:0012270] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased muscle glycogen content
in dataset: phenotype

Melanocytic nevus [hp:0000995]
type: SIO_010056
comment: Phenotype [hp:0000995] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Melanocytic nevus
in dataset: phenotype

Truncus arteriosus [hp:0001660]
type: SIO_010056
comment: Phenotype [hp:0001660] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Truncus arteriosus
in dataset: phenotype

Palmoplantar keratoderma [hp:0000982]
type: SIO_010056
comment: Phenotype [hp:0000982] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palmoplantar keratoderma
in dataset: phenotype

Stage 5 chronic kidney disease [hp:0003774]
type: SIO_010056
comment: Phenotype [hp:0003774] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stage 5 chronic kidney disease
in dataset: phenotype

Absent speech [hp:0001344]
type: SIO_010056
comment: Phenotype [hp:0001344] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent speech
in dataset: phenotype

Increased lacrimation [hp:0009926]
type: SIO_010056
comment: Phenotype [hp:0009926] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased lacrimation
in dataset: phenotype

Asymmetry of the thorax [hp:0001555]
type: SIO_010056
comment: Phenotype [hp:0001555] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Asymmetry of the thorax
in dataset: phenotype

Abnormality of blood and blood-forming tissues [hp:0001871]
type: SIO_010056
comment: Phenotype [hp:0001871] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of blood and blood-forming tissues
in dataset: phenotype

Chronic lactic acidosis [hp:0004925]
type: SIO_010056
comment: Phenotype [hp:0004925] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic lactic acidosis
in dataset: phenotype

Hypoplastic superior helix [hp:0008559]
type: SIO_010056
comment: Phenotype [hp:0008559] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic superior helix
in dataset: phenotype

Abnormal upper motor neuron morphology [hp:0002127]
type: SIO_010056
comment: Phenotype [hp:0002127] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal upper motor neuron morphology
in dataset: phenotype

Arterial tortuosity [hp:0005116]
type: SIO_010056
comment: Phenotype [hp:0005116] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arterial tortuosity
in dataset: phenotype

Dehydration [hp:0001944]
type: SIO_010056
comment: Phenotype [hp:0001944] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dehydration
in dataset: phenotype

Spinous keratoses of palms and soles [hp:0007613]
type: SIO_010056
comment: Phenotype [hp:0007613] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinous keratoses of palms and soles
in dataset: phenotype

Halberd-shaped pelvis [hp:0002826]
type: SIO_010056
comment: Phenotype [hp:0002826] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Halberd-shaped pelvis
in dataset: phenotype

Acute episodes of neuropathic symptoms [hp:0003489]
type: SIO_010056
comment: Phenotype [hp:0003489] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute episodes of neuropathic symptoms
in dataset: phenotype

Albuminuria [hp:0012592]
type: SIO_010056
comment: Phenotype [hp:0012592] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Albuminuria
in dataset: phenotype

Pectoralis amyotrophy [hp:0012037]
type: SIO_010056
comment: Phenotype [hp:0012037] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pectoralis amyotrophy
in dataset: phenotype

Sclerosis of hand bone [hp:0004054]
type: SIO_010056
comment: Phenotype [hp:0004054] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sclerosis of hand bone
in dataset: phenotype

Osteolysis involving tarsal bones [hp:0006234]
type: SIO_010056
comment: Phenotype [hp:0006234] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteolysis involving tarsal bones
in dataset: phenotype

Migraine with aura [hp:0002077]
type: SIO_010056
comment: Phenotype [hp:0002077] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Migraine with aura
in dataset: phenotype

Subacute progressive viral hepatitis [hp:0006572]
type: SIO_010056
comment: Phenotype [hp:0006572] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subacute progressive viral hepatitis
in dataset: phenotype

Aplasia of the sweat glands [hp:0011136]
type: SIO_010056
comment: Phenotype [hp:0011136] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the sweat glands
in dataset: phenotype

Episodic upper airway obstruction [hp:0012271]
type: SIO_010056
comment: Phenotype [hp:0012271] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic upper airway obstruction
in dataset: phenotype

Aplasia/Hypoplasia of the capital femoral epiphysis [hp:0005003]
type: SIO_010056
comment: Phenotype [hp:0005003] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the capital femoral epiphysis
in dataset: phenotype

Retinal thinning [hp:0030329]
type: SIO_010056
comment: Phenotype [hp:0030329] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal thinning
in dataset: phenotype

Rectoperineal fistula [hp:0004792]
type: SIO_010056
comment: Phenotype [hp:0004792] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rectoperineal fistula
in dataset: phenotype

Increased circulating gonadotropin level [hp:0000837]
type: SIO_010056
comment: Phenotype [hp:0000837] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased circulating gonadotropin level
in dataset: phenotype

Platybasia [hp:0002691]
type: SIO_010056
comment: Phenotype [hp:0002691] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Platybasia
in dataset: phenotype

Acroosteolysis of distal phalanges (feet) [hp:0001870]
type: SIO_010056
comment: Phenotype [hp:0001870] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acroosteolysis of distal phalanges (feet)
in dataset: phenotype

Narrow palate [hp:0000189]
type: SIO_010056
comment: Phenotype [hp:0000189] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow palate
in dataset: phenotype

Colpocephaly [hp:0030048]
type: SIO_010056
comment: Phenotype [hp:0030048] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Colpocephaly
in dataset: phenotype

Chilblain lesions [hp:0009710]
type: SIO_010056
comment: Phenotype [hp:0009710] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chilblain lesions
in dataset: phenotype

Phacodonesis [hp:0012629]
type: SIO_010056
comment: Phenotype [hp:0012629] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Phacodonesis
in dataset: phenotype

Primary hypothyroidism [hp:0000832]
type: SIO_010056
comment: Phenotype [hp:0000832] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Primary hypothyroidism
in dataset: phenotype

Hyperextensibility at wrists [hp:0005072]
type: SIO_010056
comment: Phenotype [hp:0005072] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperextensibility at wrists
in dataset: phenotype

Facial capillary hemangioma [hp:0000996]
type: SIO_010056
comment: Phenotype [hp:0000996] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial capillary hemangioma
in dataset: phenotype

Calcaneonavicular fusion [hp:0008122]
type: SIO_010056
comment: Phenotype [hp:0008122] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcaneonavicular fusion
in dataset: phenotype

Duane anomaly [hp:0009921]
type: SIO_010056
comment: Phenotype [hp:0009921] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Duane anomaly
in dataset: phenotype

Presacral teratoma [hp:0009793]
type: SIO_010056
comment: Phenotype [hp:0009793] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Presacral teratoma
in dataset: phenotype

Upper limb muscle weakness [hp:0003484]
type: SIO_010056
comment: Phenotype [hp:0003484] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Upper limb muscle weakness
in dataset: phenotype

Teratoma [hp:0009792]
type: SIO_010056
comment: Phenotype [hp:0009792] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Teratoma
in dataset: phenotype

Chorea [hp:0002072]
type: SIO_010056
comment: Phenotype [hp:0002072] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chorea
in dataset: phenotype

Hamartomatous stomach polyps [hp:0004795]
type: SIO_010056
comment: Phenotype [hp:0004795] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hamartomatous stomach polyps
in dataset: phenotype

J wave [hp:0012272]
type: SIO_010056
comment: Phenotype [hp:0012272] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: J wave
in dataset: phenotype

Synovial hypertrophy [hp:0005186]
type: SIO_010056
comment: Phenotype [hp:0005186] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Synovial hypertrophy
in dataset: phenotype

GM2-ganglioside accumulation [hp:0003495]
type: SIO_010056
comment: Phenotype [hp:0003495] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: GM2-ganglioside accumulation
in dataset: phenotype

Cystinuria [hp:0003131]
type: SIO_010056
comment: Phenotype [hp:0003131] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cystinuria
in dataset: phenotype

Difficulty standing [hp:0003698]
type: SIO_010056
comment: Phenotype [hp:0003698] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Difficulty standing
in dataset: phenotype

Short fifth metatarsal [hp:0004704]
type: SIO_010056
comment: Phenotype [hp:0004704] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short fifth metatarsal
in dataset: phenotype

Swan neck-like deformities of the fingers [hp:0006150]
type: SIO_010056
comment: Phenotype [hp:0006150] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Swan neck-like deformities of the fingers
in dataset: phenotype

Corneal guttata [hp:0012038]
type: SIO_010056
comment: Phenotype [hp:0012038] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corneal guttata
in dataset: phenotype

Prolonged neonatal jaundice [hp:0006579]
type: SIO_010056
comment: Phenotype [hp:0006579] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolonged neonatal jaundice
in dataset: phenotype

Violent behavior [hp:0008760]
type: SIO_010056
comment: Phenotype [hp:0008760] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Violent behavior
in dataset: phenotype

Hypoplastic facial bones [hp:0002692]
type: SIO_010056
comment: Phenotype [hp:0002692] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic facial bones
in dataset: phenotype

Aminoglycoside-induced hearing loss [hp:0011975]
type: SIO_010056
comment: Phenotype [hp:0011975] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aminoglycoside-induced hearing loss
in dataset: phenotype

Short upper lip [hp:0000188]
type: SIO_010056
comment: Phenotype [hp:0000188] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short upper lip
in dataset: phenotype

1-3 toe syndactyly [hp:0001459]
type: SIO_010056
comment: Phenotype [hp:0001459] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 1-3 toe syndactyly
in dataset: phenotype

Prenatal movement abnormality [hp:0001557]
type: SIO_010056
comment: Phenotype [hp:0001557] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prenatal movement abnormality
in dataset: phenotype

Distal/middle symphalangism of 5th finger [hp:0009244]
type: SIO_010056
comment: Phenotype [hp:0009244] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal/middle symphalangism of 5th finger
in dataset: phenotype

Insulin-resistant diabetes mellitus [hp:0000831]
type: SIO_010056
comment: Phenotype [hp:0000831] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Insulin-resistant diabetes mellitus
in dataset: phenotype

Retinal hemangioblastoma [hp:0009711]
type: SIO_010056
comment: Phenotype [hp:0009711] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal hemangioblastoma
in dataset: phenotype

Limb ataxia [hp:0002070]
type: SIO_010056
comment: Phenotype [hp:0002070] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb ataxia
in dataset: phenotype

Gynecomastia [hp:0000771]
type: SIO_010056
comment: Phenotype [hp:0000771] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gynecomastia
in dataset: phenotype

Axillary freckling [hp:0000997]
type: SIO_010056
comment: Phenotype [hp:0000997] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Axillary freckling
in dataset: phenotype

Malrotation of small bowel [hp:0004794]
type: SIO_010056
comment: Phenotype [hp:0004794] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malrotation of small bowel
in dataset: phenotype

Bifid sacrum [hp:0009791]
type: SIO_010056
comment: Phenotype [hp:0009791] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid sacrum
in dataset: phenotype

Abnormality of extrapyramidal motor function [hp:0002071]
type: SIO_010056
comment: Phenotype [hp:0002071] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of extrapyramidal motor function
in dataset: phenotype

Recurrent deep vein thrombosis [hp:0004850]
type: SIO_010056
comment: Phenotype [hp:0004850] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent deep vein thrombosis
in dataset: phenotype

Limited extraocular movements [hp:0007941]
type: SIO_010056
comment: Phenotype [hp:0007941] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited extraocular movements
in dataset: phenotype

Recurrent systemic pyogenic infections [hp:0005429]
type: SIO_010056
comment: Phenotype [hp:0005429] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent systemic pyogenic infections
in dataset: phenotype

Increased IgM level [hp:0003496]
type: SIO_010056
comment: Phenotype [hp:0003496] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased IgM level
in dataset: phenotype

Increased carotid artery intimal medial thickness [hp:0012273]
type: SIO_010056
comment: Phenotype [hp:0012273] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased carotid artery intimal medial thickness
in dataset: phenotype

Unilateral vestibular Schwannoma [hp:0009590]
type: SIO_010056
comment: Phenotype [hp:0009590] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral vestibular Schwannoma
in dataset: phenotype

Nystagmus [hp:0000639]
type: SIO_010056
comment: Phenotype [hp:0000639] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nystagmus
in dataset: phenotype

Scapuloperoneal amyotrophy [hp:0003697]
type: SIO_010056
comment: Phenotype [hp:0003697] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scapuloperoneal amyotrophy
in dataset: phenotype

Descemet Membrane Folds [hp:0012039]
type: SIO_010056
comment: Phenotype [hp:0012039] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Descemet Membrane Folds
in dataset: phenotype

Abnormal peripheral myelination [hp:0003130]
type: SIO_010056
comment: Phenotype [hp:0003130] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal peripheral myelination
in dataset: phenotype

Aplastic anemia [hp:0001915]
type: SIO_010056
comment: Phenotype [hp:0001915] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplastic anemia
in dataset: phenotype

Retrocerebellar cyst [hp:0006951]
type: SIO_010056
comment: Phenotype [hp:0006951] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retrocerebellar cyst
in dataset: phenotype

Brain abscess [hp:0030049]
type: SIO_010056
comment: Phenotype [hp:0030049] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Brain abscess
in dataset: phenotype

Ventral hernia [hp:0002933]
type: SIO_010056
comment: Phenotype [hp:0002933] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ventral hernia
in dataset: phenotype

Hypopigmentation of the skin [hp:0001010]
type: SIO_010056
comment: Phenotype [hp:0001010] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypopigmentation of the skin
in dataset: phenotype

Psychomotor deterioration [hp:0002361]
type: SIO_010056
comment: Phenotype [hp:0002361] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Psychomotor deterioration
in dataset: phenotype

Decreased fetal movement [hp:0001558]
type: SIO_010056
comment: Phenotype [hp:0001558] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased fetal movement
in dataset: phenotype

Pulp stones [hp:0003771]
type: SIO_010056
comment: Phenotype [hp:0003771] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulp stones
in dataset: phenotype

Progressive loss of facial adipose tissue [hp:0009019]
type: SIO_010056
comment: Phenotype [hp:0009019] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive loss of facial adipose tissue
in dataset: phenotype

Progressive reticulate hyperpigmentation [hp:0007456]
type: SIO_010056
comment: Phenotype [hp:0007456] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive reticulate hyperpigmentation
in dataset: phenotype

Peripheral arterial stenosis [hp:0004928]
type: SIO_010056
comment: Phenotype [hp:0004928] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral arterial stenosis
in dataset: phenotype

Neuropathic arthropathy [hp:0002821]
type: SIO_010056
comment: Phenotype [hp:0002821] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neuropathic arthropathy
in dataset: phenotype

Abnormality of the ribs [hp:0000772]
type: SIO_010056
comment: Phenotype [hp:0000772] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the ribs
in dataset: phenotype

Anterior rounding of vertebral bodies [hp:0008488]
type: SIO_010056
comment: Phenotype [hp:0008488] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior rounding of vertebral bodies
in dataset: phenotype

Pericardial lymphangiectasia [hp:0005183]
type: SIO_010056
comment: Phenotype [hp:0005183] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pericardial lymphangiectasia
in dataset: phenotype

Olfactory lobe agenesis [hp:0001341]
type: SIO_010056
comment: Phenotype [hp:0001341] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Olfactory lobe agenesis
in dataset: phenotype

Severe recurrent varicella [hp:0005428]
type: SIO_010056
comment: Phenotype [hp:0005428] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe recurrent varicella
in dataset: phenotype

Abnormality of the adrenal glands [hp:0000834]
type: SIO_010056
comment: Phenotype [hp:0000834] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the adrenal glands
in dataset: phenotype

Mild proteinuria [hp:0012595]
type: SIO_010056
comment: Phenotype [hp:0012595] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mild proteinuria
in dataset: phenotype

Death in childhood [hp:0003819]
type: SIO_010056
comment: Phenotype [hp:0003819] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Death in childhood
in dataset: phenotype

Prolonged QTc interval [hp:0005184]
type: SIO_010056
comment: Phenotype [hp:0005184] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolonged QTc interval
in dataset: phenotype

Atypical scarring of skin [hp:0000987]
type: SIO_010056
comment: Phenotype [hp:0000987] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atypical scarring of skin
in dataset: phenotype

Hemisacrum (S2-S5) [hp:0009790]
type: SIO_010056
comment: Phenotype [hp:0009790] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemisacrum (S2-S5)
in dataset: phenotype

Increased neuronal autofluorescent lipopigment [hp:0002074]
type: SIO_010056
comment: Phenotype [hp:0002074] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased neuronal autofluorescent lipopigment
in dataset: phenotype

Blotching pigmentation of the skin [hp:0007610]
type: SIO_010056
comment: Phenotype [hp:0007610] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Blotching pigmentation of the skin
in dataset: phenotype

Hypertrichosis [hp:0000998]
type: SIO_010056
comment: Phenotype [hp:0000998] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertrichosis
in dataset: phenotype

Elevated urinary vanillylmandelic acid [hp:0011978]
type: SIO_010056
comment: Phenotype [hp:0011978] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated urinary vanillylmandelic acid
in dataset: phenotype

Prominent interphalangeal joints [hp:0006237]
type: SIO_010056
comment: Phenotype [hp:0006237] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent interphalangeal joints
in dataset: phenotype

Hypokalemic alkalosis [hp:0001949]
type: SIO_010056
comment: Phenotype [hp:0001949] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypokalemic alkalosis
in dataset: phenotype

Large sella turcica [hp:0002690]
type: SIO_010056
comment: Phenotype [hp:0002690] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large sella turcica
in dataset: phenotype

Coronary atherosclerosis [hp:0004929]
type: SIO_010056
comment: Phenotype [hp:0004929] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coronary atherosclerosis
in dataset: phenotype

Cone-shaped epiphyses of the middle phalanges of the hand [hp:0010259]
type: SIO_010056
comment: Phenotype [hp:0010259] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cone-shaped epiphyses of the middle phalanges of the hand
in dataset: phenotype

Aldehyde oxidase deficiency [hp:0002932]
type: SIO_010056
comment: Phenotype [hp:0002932] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aldehyde oxidase deficiency
in dataset: phenotype

Spinal hemangioblastoma [hp:0009713]
type: SIO_010056
comment: Phenotype [hp:0009713] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinal hemangioblastoma
in dataset: phenotype

Adermatoglyphia [hp:0007455]
type: SIO_010056
comment: Phenotype [hp:0007455] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adermatoglyphia
in dataset: phenotype

Sleep disturbance [hp:0002360]
type: SIO_010056
comment: Phenotype [hp:0002360] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sleep disturbance
in dataset: phenotype

Hyperplasia of the femoral trochanters [hp:0002822]
type: SIO_010056
comment: Phenotype [hp:0002822] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperplasia of the femoral trochanters
in dataset: phenotype

Spinal cord lesion [hp:0100561]
type: SIO_010056
comment: Phenotype [hp:0100561] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinal cord lesion
in dataset: phenotype

Morphological abnormality of the middle ear [hp:0008609]
type: SIO_010056
comment: Phenotype [hp:0008609] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Morphological abnormality of the middle ear
in dataset: phenotype

Short ribs [hp:0000773]
type: SIO_010056
comment: Phenotype [hp:0000773] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short ribs
in dataset: phenotype

Reduced catalase activity [hp:0012517]
type: SIO_010056
comment: Phenotype [hp:0012517] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced catalase activity
in dataset: phenotype

Enhancement of the C-reflex [hp:0001340]
type: SIO_010056
comment: Phenotype [hp:0001340] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enhancement of the C-reflex
in dataset: phenotype

Enuresis nocturna [hp:0010677]
type: SIO_010056
comment: Phenotype [hp:0010677] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enuresis nocturna
in dataset: phenotype

Autosomal dominant inheritance with maternal imprinting [hp:0012275]
type: SIO_010056
comment: Phenotype [hp:0012275] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autosomal dominant inheritance with maternal imprinting
in dataset: phenotype

Glucose intolerance [hp:0000833]
type: SIO_010056
comment: Phenotype [hp:0000833] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glucose intolerance
in dataset: phenotype

Pyoderma [hp:0000999]
type: SIO_010056
comment: Phenotype [hp:0000999] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pyoderma
in dataset: phenotype

Lumbar scoliosis [hp:0004626]
type: SIO_010056
comment: Phenotype [hp:0004626] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lumbar scoliosis
in dataset: phenotype

Calf muscle pseudohypertrophy [hp:0003707]
type: SIO_010056
comment: Phenotype [hp:0003707] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calf muscle pseudohypertrophy
in dataset: phenotype

Hepatic vascular malformations [hp:0006576]
type: SIO_010056
comment: Phenotype [hp:0006576] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatic vascular malformations
in dataset: phenotype

Progressive cerebellar ataxia [hp:0002073]
type: SIO_010056
comment: Phenotype [hp:0002073] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive cerebellar ataxia
in dataset: phenotype

Elevated urinary homovanillic acid [hp:0011977]
type: SIO_010056
comment: Phenotype [hp:0011977] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated urinary homovanillic acid
in dataset: phenotype

Long palpebral fissure [hp:0000637]
type: SIO_010056
comment: Phenotype [hp:0000637] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long palpebral fissure
in dataset: phenotype

Gastrointestinal obstruction [hp:0004796]
type: SIO_010056
comment: Phenotype [hp:0004796] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gastrointestinal obstruction
in dataset: phenotype

Disproportionate short stature [hp:0003498]
type: SIO_010056
comment: Phenotype [hp:0003498] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Disproportionate short stature
in dataset: phenotype

Alkalosis [hp:0001948]
type: SIO_010056
comment: Phenotype [hp:0001948] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Alkalosis
in dataset: phenotype

Aplasia of the tarsal bones [hp:0010509]
type: SIO_010056
comment: Phenotype [hp:0010509] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the tarsal bones
in dataset: phenotype

Congenital stapes ankylosis [hp:0007943]
type: SIO_010056
comment: Phenotype [hp:0007943] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital stapes ankylosis
in dataset: phenotype

Granulocytopenia [hp:0001913]
type: SIO_010056
comment: Phenotype [hp:0001913] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Granulocytopenia
in dataset: phenotype

Thromboembolism [hp:0001907]
type: SIO_010056
comment: Phenotype [hp:0001907] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thromboembolism
in dataset: phenotype

Aplasia/Hypoplasia of the thymus [hp:0010515]
type: SIO_010056
comment: Phenotype [hp:0010515] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the thymus
in dataset: phenotype

Madelung-like forearm deformities [hp:0003068]
type: SIO_010056
comment: Phenotype [hp:0003068] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Madelung-like forearm deformities
in dataset: phenotype

Ciliary dyskinesia [hp:0012265]
type: SIO_010056
comment: Phenotype [hp:0012265] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ciliary dyskinesia
in dataset: phenotype

Regional abnormality of skin [hp:0011356]
type: SIO_010056
comment: Phenotype [hp:0011356] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Regional abnormality of skin
in dataset: phenotype

Giant cell hepatitis [hp:0200084]
type: SIO_010056
comment: Phenotype [hp:0200084] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Giant cell hepatitis
in dataset: phenotype

Varicose veins [hp:0002619]
type: SIO_010056
comment: Phenotype [hp:0002619] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Varicose veins
in dataset: phenotype

Recurrent infections in infancy and early childhood [hp:0005437]
type: SIO_010056
comment: Phenotype [hp:0005437] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent infections in infancy and early childhood
in dataset: phenotype

Diffuse spongiform leukoencephalopathy [hp:0006943]
type: SIO_010056
comment: Phenotype [hp:0006943] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse spongiform leukoencephalopathy
in dataset: phenotype

Heterotopia [hp:0002282]
type: SIO_010056
comment: Phenotype [hp:0002282] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Heterotopia
in dataset: phenotype

Thickened calvaria [hp:0002684]
type: SIO_010056
comment: Phenotype [hp:0002684] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thickened calvaria
in dataset: phenotype

Hypopigmented streaks [hp:0007535]
type: SIO_010056
comment: Phenotype [hp:0007535] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypopigmented streaks
in dataset: phenotype

Dislocated wrist [hp:0003994]
type: SIO_010056
comment: Phenotype [hp:0003994] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dislocated wrist
in dataset: phenotype

Extrapyramidal dyskinesia [hp:0007308]
type: SIO_010056
comment: Phenotype [hp:0007308] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Extrapyramidal dyskinesia
in dataset: phenotype

Bilateral sensorineural hearing impairment [hp:0008619]
type: SIO_010056
comment: Phenotype [hp:0008619] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral sensorineural hearing impairment
in dataset: phenotype

Radial deviation of finger [hp:0009466]
type: SIO_010056
comment: Phenotype [hp:0009466] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Radial deviation of finger
in dataset: phenotype

Lower lip pit [hp:0000196]
type: SIO_010056
comment: Phenotype [hp:0000196] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lower lip pit
in dataset: phenotype

Abnormality of the diaphragm [hp:0000775]
type: SIO_010056
comment: Phenotype [hp:0000775] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the diaphragm
in dataset: phenotype

Posterior polar cataract [hp:0001115]
type: SIO_010056
comment: Phenotype [hp:0001115] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior polar cataract
in dataset: phenotype

Oligosacchariduria [hp:0010471]
type: SIO_010056
comment: Phenotype [hp:0010471] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oligosacchariduria
in dataset: phenotype

Ectopic kidney [hp:0000086]
type: SIO_010056
comment: Phenotype [hp:0000086] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopic kidney
in dataset: phenotype

Broad phalanx [hp:0006009]
type: SIO_010056
comment: Phenotype [hp:0006009] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad phalanx
in dataset: phenotype

Flexural lichenification [hp:0007453]
type: SIO_010056
comment: Phenotype [hp:0007453] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flexural lichenification
in dataset: phenotype

Premature separation of centromeric heterochromatin [hp:0003616]
type: SIO_010056
comment: Phenotype [hp:0003616] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature separation of centromeric heterochromatin
in dataset: phenotype

1-5 finger complete cutaneous syndactyly [hp:0006088]
type: SIO_010056
comment: Phenotype [hp:0006088] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 1-5 finger complete cutaneous syndactyly
in dataset: phenotype

Thymus hyperplasia [hp:0010516]
type: SIO_010056
comment: Phenotype [hp:0010516] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thymus hyperplasia
in dataset: phenotype

Fulminant hepatitis [hp:0004787]
type: SIO_010056
comment: Phenotype [hp:0004787] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fulminant hepatitis
in dataset: phenotype

Short middle phalanx of the 5th finger [hp:0004220]
type: SIO_010056
comment: Phenotype [hp:0004220] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short middle phalanx of the 5th finger
in dataset: phenotype

Premature pubarche [hp:0012411]
type: SIO_010056
comment: Phenotype [hp:0012411] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature pubarche
in dataset: phenotype

Hypoplastic olfactory lobes [hp:0006894]
type: SIO_010056
comment: Phenotype [hp:0006894] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic olfactory lobes
in dataset: phenotype

Bilateral congenital mydriasis [hp:0007932]
type: SIO_010056
comment: Phenotype [hp:0007932] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral congenital mydriasis
in dataset: phenotype

Madelung deformity [hp:0003067]
type: SIO_010056
comment: Phenotype [hp:0003067] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Madelung deformity
in dataset: phenotype

Severe limb shortening [hp:0200083]
type: SIO_010056
comment: Phenotype [hp:0200083] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe limb shortening
in dataset: phenotype

Radial club hand [hp:0004059]
type: SIO_010056
comment: Phenotype [hp:0004059] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Radial club hand
in dataset: phenotype

Aglossia [hp:0012730]
type: SIO_010056
comment: Phenotype [hp:0012730] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aglossia
in dataset: phenotype

Localized skin lesion [hp:0011355]
type: SIO_010056
comment: Phenotype [hp:0011355] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Localized skin lesion
in dataset: phenotype

Gray matter heterotopias [hp:0002281]
type: SIO_010056
comment: Phenotype [hp:0002281] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gray matter heterotopias
in dataset: phenotype

Ulnar deviation of finger [hp:0009465]
type: SIO_010056
comment: Phenotype [hp:0009465] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ulnar deviation of finger
in dataset: phenotype

Abnormality of parotid gland [hp:0000197]
type: SIO_010056
comment: Phenotype [hp:0000197] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of parotid gland
in dataset: phenotype

Frequent falls [hp:0002359]
type: SIO_010056
comment: Phenotype [hp:0002359] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frequent falls
in dataset: phenotype

Xanthelasma [hp:0001114]
type: SIO_010056
comment: Phenotype [hp:0001114] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Xanthelasma
in dataset: phenotype

Abnormality of branched chain family amino acid metabolism [hp:0010892]
type: SIO_010056
comment: Phenotype [hp:0010892] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of branched chain family amino acid metabolism
in dataset: phenotype

Narrow chest [hp:0000774]
type: SIO_010056
comment: Phenotype [hp:0000774] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow chest
in dataset: phenotype

Horseshoe kidney [hp:0000085]
type: SIO_010056
comment: Phenotype [hp:0000085] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Horseshoe kidney
in dataset: phenotype

Hypoplasia of the fallopian tube [hp:0008697]
type: SIO_010056
comment: Phenotype [hp:0008697] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the fallopian tube
in dataset: phenotype

Excessive salivation [hp:0003781]
type: SIO_010056
comment: Phenotype [hp:0003781] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Excessive salivation
in dataset: phenotype

Abnormality of skin pigmentation [hp:0001000]
type: SIO_010056
comment: Phenotype [hp:0001000] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of skin pigmentation
in dataset: phenotype

Auditory hallucinations [hp:0008765]
type: SIO_010056
comment: Phenotype [hp:0008765] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Auditory hallucinations
in dataset: phenotype

Anal mucosal leukoplakia [hp:0005212]
type: SIO_010056
comment: Phenotype [hp:0005212] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anal mucosal leukoplakia
in dataset: phenotype

Ectopic thymus tissue [hp:0010517]
type: SIO_010056
comment: Phenotype [hp:0010517] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopic thymus tissue
in dataset: phenotype

Thick cerebral cortex [hp:0006891]
type: SIO_010056
comment: Phenotype [hp:0006891] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thick cerebral cortex
in dataset: phenotype

Abnormality of eosinophils [hp:0001879]
type: SIO_010056
comment: Phenotype [hp:0001879] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of eosinophils
in dataset: phenotype

Increased prevalence of valvular disease [hp:0001726]
type: SIO_010056
comment: Phenotype [hp:0001726] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased prevalence of valvular disease
in dataset: phenotype

Juvenile posterior subcapsular lenticular opacities [hp:0007935]
type: SIO_010056
comment: Phenotype [hp:0007935] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Juvenile posterior subcapsular lenticular opacities
in dataset: phenotype

Congenital thrombocytopenia [hp:0001905]
type: SIO_010056
comment: Phenotype [hp:0001905] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital thrombocytopenia
in dataset: phenotype

Hurthle cell thyroid adenoma [hp:0006781]
type: SIO_010056
comment: Phenotype [hp:0006781] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hurthle cell thyroid adenoma
in dataset: phenotype

Trimethylaminuria [hp:0003614]
type: SIO_010056
comment: Phenotype [hp:0003614] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Trimethylaminuria
in dataset: phenotype

Impaired T cell function [hp:0005435]
type: SIO_010056
comment: Phenotype [hp:0005435] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired T cell function
in dataset: phenotype

Abnormality of the anus [hp:0004378]
type: SIO_010056
comment: Phenotype [hp:0004378] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the anus
in dataset: phenotype

Extension of hair growth on temples to lateral eyebrow [hp:0005325]
type: SIO_010056
comment: Phenotype [hp:0005325] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Extension of hair growth on temples to lateral eyebrow
in dataset: phenotype

Aneurysm [hp:0002617]
type: SIO_010056
comment: Phenotype [hp:0002617] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aneurysm
in dataset: phenotype

Episodic ataxia [hp:0002131]
type: SIO_010056
comment: Phenotype [hp:0002131] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic ataxia
in dataset: phenotype

Microtia [hp:0008551]
type: SIO_010056
comment: Phenotype [hp:0008551] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microtia
in dataset: phenotype

Acral ulceration and osteomyelitis leading to autoamputation of digits [hp:0001226]
type: SIO_010056
comment: Phenotype [hp:0001226] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acral ulceration and osteomyelitis leading to autoamputation of digits
in dataset: phenotype

Abnormality of the thymus [hp:0000777]
type: SIO_010056
comment: Phenotype [hp:0000777] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the thymus
in dataset: phenotype

Morbus Scheuermann [hp:0010891]
type: SIO_010056
comment: Phenotype [hp:0010891] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Morbus Scheuermann
in dataset: phenotype

Ulnar deviation of the 2nd finger [hp:0009464]
type: SIO_010056
comment: Phenotype [hp:0009464] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ulnar deviation of the 2nd finger
in dataset: phenotype

Slender ulna [hp:0003992]
type: SIO_010056
comment: Phenotype [hp:0003992] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slender ulna
in dataset: phenotype

Repetitive compulsive behavior [hp:0008762]
type: SIO_010056
comment: Phenotype [hp:0008762] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Repetitive compulsive behavior
in dataset: phenotype

Absence of Stensen duct [hp:0000198]
type: SIO_010056
comment: Phenotype [hp:0000198] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of Stensen duct
in dataset: phenotype

Broad skull [hp:0002682]
type: SIO_010056
comment: Phenotype [hp:0002682] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad skull
in dataset: phenotype

Hypoproteinemic edema [hp:0007609]
type: SIO_010056
comment: Phenotype [hp:0007609] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoproteinemic edema
in dataset: phenotype

Porphyrinuria [hp:0010473]
type: SIO_010056
comment: Phenotype [hp:0010473] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Porphyrinuria
in dataset: phenotype

Progressive central visual loss [hp:0008008]
type: SIO_010056
comment: Phenotype [hp:0008008] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive central visual loss
in dataset: phenotype

Thromboembolic stroke [hp:0001727]
type: SIO_010056
comment: Phenotype [hp:0001727] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thromboembolic stroke
in dataset: phenotype

Midgut malrotation [hp:0005211]
type: SIO_010056
comment: Phenotype [hp:0005211] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Midgut malrotation
in dataset: phenotype

Frontotemporal cerebral atrophy [hp:0006892]
type: SIO_010056
comment: Phenotype [hp:0006892] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontotemporal cerebral atrophy
in dataset: phenotype

T-wave alternans [hp:0012266]
type: SIO_010056
comment: Phenotype [hp:0012266] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: T-wave alternans
in dataset: phenotype

Lactose intolerance [hp:0004789]
type: SIO_010056
comment: Phenotype [hp:0004789] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lactose intolerance
in dataset: phenotype

Autoimmune neutropenia [hp:0001904]
type: SIO_010056
comment: Phenotype [hp:0001904] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autoimmune neutropenia
in dataset: phenotype

Parathyroid carcinoma [hp:0006780]
type: SIO_010056
comment: Phenotype [hp:0006780] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Parathyroid carcinoma
in dataset: phenotype

Antiphospholipid antibody positivity [hp:0003613]
type: SIO_010056
comment: Phenotype [hp:0003613] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Antiphospholipid antibody positivity
in dataset: phenotype

Abnormality of alkaline phosphatase activity [hp:0004379]
type: SIO_010056
comment: Phenotype [hp:0004379] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of alkaline phosphatase activity
in dataset: phenotype

Radial deviation of the 3rd finger [hp:0009462]
type: SIO_010056
comment: Phenotype [hp:0009462] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Radial deviation of the 3rd finger
in dataset: phenotype

Global brain atrophy [hp:0002283]
type: SIO_010056
comment: Phenotype [hp:0002283] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Global brain atrophy
in dataset: phenotype

Arterial intimal fibrosis [hp:0011353]
type: SIO_010056
comment: Phenotype [hp:0011353] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arterial intimal fibrosis
in dataset: phenotype

Corneal stromal edema [hp:0012040]
type: SIO_010056
comment: Phenotype [hp:0012040] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corneal stromal edema
in dataset: phenotype

Disturbance of facial expression [hp:0005324]
type: SIO_010056
comment: Phenotype [hp:0005324] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Disturbance of facial expression
in dataset: phenotype

Limb tremor [hp:0200085]
type: SIO_010056
comment: Phenotype [hp:0200085] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb tremor
in dataset: phenotype

Primary congenital glaucoma [hp:0008007]
type: SIO_010056
comment: Phenotype [hp:0008007] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Primary congenital glaucoma
in dataset: phenotype

Osteopathia striata [hp:0010740]
type: SIO_010056
comment: Phenotype [hp:0010740] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteopathia striata
in dataset: phenotype

Decreased subcutaneous fat [hp:0001002]
type: SIO_010056
comment: Phenotype [hp:0001002] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased subcutaneous fat
in dataset: phenotype

Unilateral brachydactyly [hp:0006008]
type: SIO_010056
comment: Phenotype [hp:0006008] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral brachydactyly
in dataset: phenotype

Congenital diaphragmatic hernia [hp:0000776]
type: SIO_010056
comment: Phenotype [hp:0000776] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital diaphragmatic hernia
in dataset: phenotype

Rapid neurologic deterioration [hp:0007307]
type: SIO_010056
comment: Phenotype [hp:0007307] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rapid neurologic deterioration
in dataset: phenotype

Wrist swelling [hp:0001225]
type: SIO_010056
comment: Phenotype [hp:0001225] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Wrist swelling
in dataset: phenotype

Leber optic atrophy [hp:0001112]
type: SIO_010056
comment: Phenotype [hp:0001112] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Leber optic atrophy
in dataset: phenotype

Broad ulna [hp:0003993]
type: SIO_010056
comment: Phenotype [hp:0003993] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad ulna
in dataset: phenotype

Renal insufficiency [hp:0000083]
type: SIO_010056
comment: Phenotype [hp:0000083] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal insufficiency
in dataset: phenotype

Ulnar deviation of the 3rd finger [hp:0009463]
type: SIO_010056
comment: Phenotype [hp:0009463] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ulnar deviation of the 3rd finger
in dataset: phenotype

Palmar hyperhidrosis [hp:0006089]
type: SIO_010056
comment: Phenotype [hp:0006089] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palmar hyperhidrosis
in dataset: phenotype

Tongue nodules [hp:0000199]
type: SIO_010056
comment: Phenotype [hp:0000199] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tongue nodules
in dataset: phenotype

Deformed sella turcica [hp:0002681]
type: SIO_010056
comment: Phenotype [hp:0002681] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deformed sella turcica
in dataset: phenotype

No social interaction [hp:0008763]
type: SIO_010056
comment: Phenotype [hp:0008763] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: No social interaction
in dataset: phenotype

Midface capillary hemangioma [hp:0007452]
type: SIO_010056
comment: Phenotype [hp:0007452] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Midface capillary hemangioma
in dataset: phenotype

Abnormality of the heme biosynthetic pathway [hp:0010472]
type: SIO_010056
comment: Phenotype [hp:0010472] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the heme biosynthetic pathway
in dataset: phenotype

Status epilepticus [hp:0002133]
type: SIO_010056
comment: Phenotype [hp:0002133] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Status epilepticus
in dataset: phenotype

Pendular nystagmus [hp:0012043]
type: SIO_010056
comment: Phenotype [hp:0012043] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pendular nystagmus
in dataset: phenotype

Hypotension [hp:0002615]
type: SIO_010056
comment: Phenotype [hp:0002615] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypotension
in dataset: phenotype

Widely spaced toes [hp:0008094]
type: SIO_010056
comment: Phenotype [hp:0008094] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Widely spaced toes
in dataset: phenotype

Loss of facial expression [hp:0005327]
type: SIO_010056
comment: Phenotype [hp:0005327] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Loss of facial expression
in dataset: phenotype

Expanded metacarpals with widened medullary cavities [hp:0006232]
type: SIO_010056
comment: Phenotype [hp:0006232] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Expanded metacarpals with widened medullary cavities
in dataset: phenotype

Short 3rd finger [hp:0009461]
type: SIO_010056
comment: Phenotype [hp:0009461] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short 3rd finger
in dataset: phenotype

Square pelvis [hp:0003278]
type: SIO_010056
comment: Phenotype [hp:0003278] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Square pelvis
in dataset: phenotype

Positive ferric chloride test [hp:0003612]
type: SIO_010056
comment: Phenotype [hp:0003612] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Positive ferric chloride test
in dataset: phenotype

Hyperphenylalaninemia [hp:0004923]
type: SIO_010056
comment: Phenotype [hp:0004923] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperphenylalaninemia
in dataset: phenotype

Honeycomb retinal degeneration [hp:0007937]
type: SIO_010056
comment: Phenotype [hp:0007937] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Honeycomb retinal degeneration
in dataset: phenotype

Posterior pharyngeal cleft [hp:0006783]
type: SIO_010056
comment: Phenotype [hp:0006783] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior pharyngeal cleft
in dataset: phenotype

Hypohidrotic ectodermal dysplasia [hp:0007607]
type: SIO_010056
comment: Phenotype [hp:0007607] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypohidrotic ectodermal dysplasia
in dataset: phenotype

Schmorl's node [hp:0030041]
type: SIO_010056
comment: Phenotype [hp:0030041] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Schmorl's node
in dataset: phenotype

Abnormality of erythrocytes [hp:0001877]
type: SIO_010056
comment: Phenotype [hp:0001877] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of erythrocytes
in dataset: phenotype

Anisocoria [hp:0009916]
type: SIO_010056
comment: Phenotype [hp:0009916] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anisocoria
in dataset: phenotype

Hypertrophic labia minora [hp:0008694]
type: SIO_010056
comment: Phenotype [hp:0008694] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertrophic labia minora
in dataset: phenotype

Long toe [hp:0010511]
type: SIO_010056
comment: Phenotype [hp:0010511] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long toe
in dataset: phenotype

Triangular shaped proximal phalanx of the 2nd finger [hp:0009587]
type: SIO_010056
comment: Phenotype [hp:0009587] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular shaped proximal phalanx of the 2nd finger
in dataset: phenotype

Proximal muscle weakness [hp:0003701]
type: SIO_010056
comment: Phenotype [hp:0003701] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal muscle weakness
in dataset: phenotype

Memory impairment [hp:0002354]
type: SIO_010056
comment: Phenotype [hp:0002354] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Memory impairment
in dataset: phenotype

Multiple lentigines [hp:0001003]
type: SIO_010056
comment: Phenotype [hp:0001003] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple lentigines
in dataset: phenotype

Absent frontal sinuses [hp:0002688]
type: SIO_010056
comment: Phenotype [hp:0002688] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent frontal sinuses
in dataset: phenotype

Adult onset sensorineural hearing impairment [hp:0008615]
type: SIO_010056
comment: Phenotype [hp:0008615] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adult onset sensorineural hearing impairment
in dataset: phenotype

Inappropriate sexual behavior [hp:0008768]
type: SIO_010056
comment: Phenotype [hp:0008768] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inappropriate sexual behavior
in dataset: phenotype

Aspirin-induced asthma [hp:0012042]
type: SIO_010056
comment: Phenotype [hp:0012042] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aspirin-induced asthma
in dataset: phenotype

Lethal short-limbed short stature [hp:0008909]
type: SIO_010056
comment: Phenotype [hp:0008909] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lethal short-limbed short stature
in dataset: phenotype

Dry hair [hp:0011359]
type: SIO_010056
comment: Phenotype [hp:0011359] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dry hair
in dataset: phenotype

Hypoplastic philtrum [hp:0005326]
type: SIO_010056
comment: Phenotype [hp:0005326] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic philtrum
in dataset: phenotype

Prolonged QRS complex [hp:0006677]
type: SIO_010056
comment: Phenotype [hp:0006677] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolonged QRS complex
in dataset: phenotype

Reduced number of intrahepatic bile ducts [hp:0006571]
type: SIO_010056
comment: Phenotype [hp:0006571] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced number of intrahepatic bile ducts
in dataset: phenotype

Everted upper lip vermilion [hp:0010803]
type: SIO_010056
comment: Phenotype [hp:0010803] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Everted upper lip vermilion
in dataset: phenotype

Abnormality of epiphysis morphology [hp:0005930]
type: SIO_010056
comment: Phenotype [hp:0005930] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of epiphysis morphology
in dataset: phenotype

Aortic root dilatation [hp:0002616]
type: SIO_010056
comment: Phenotype [hp:0002616] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aortic root dilatation
in dataset: phenotype

Panniculitis [hp:0012490]
type: SIO_010056
comment: Phenotype [hp:0012490] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Panniculitis
in dataset: phenotype

Recurrent meningitis [hp:0006946]
type: SIO_010056
comment: Phenotype [hp:0006946] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent meningitis
in dataset: phenotype

Porencephaly [hp:0002132]
type: SIO_010056
comment: Phenotype [hp:0002132] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Porencephaly
in dataset: phenotype

Hypoplasia of the thymus [hp:0000778]
type: SIO_010056
comment: Phenotype [hp:0000778] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the thymus
in dataset: phenotype

Abnormality of the parathyroid gland [hp:0000828]
type: SIO_010056
comment: Phenotype [hp:0000828] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the parathyroid gland
in dataset: phenotype

Constricted iliac wings [hp:0003277]
type: SIO_010056
comment: Phenotype [hp:0003277] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Constricted iliac wings
in dataset: phenotype

Malignant eosinophil proliferation [hp:0006782]
type: SIO_010056
comment: Phenotype [hp:0006782] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malignant eosinophil proliferation
in dataset: phenotype

Restrictive external ophthalmoplegia [hp:0007936]
type: SIO_010056
comment: Phenotype [hp:0007936] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Restrictive external ophthalmoplegia
in dataset: phenotype

Abnormality of the humerus [hp:0003063]
type: SIO_010056
comment: Phenotype [hp:0003063] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the humerus
in dataset: phenotype

Hemolytic anemia [hp:0001878]
type: SIO_010056
comment: Phenotype [hp:0001878] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemolytic anemia
in dataset: phenotype

Myxoid liposarcoma [hp:0012268]
type: SIO_010056
comment: Phenotype [hp:0012268] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myxoid liposarcoma
in dataset: phenotype

Punctate palmoplantar hyperkeratosis [hp:0007530]
type: SIO_010056
comment: Phenotype [hp:0007530] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Punctate palmoplantar hyperkeratosis
in dataset: phenotype

Abnormality of the eyelashes [hp:0000499]
type: SIO_010056
comment: Phenotype [hp:0000499] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the eyelashes
in dataset: phenotype

Persistent pupillary membrane [hp:0009917]
type: SIO_010056
comment: Phenotype [hp:0009917] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Persistent pupillary membrane
in dataset: phenotype

Renal hypoplasia [hp:0000089]
type: SIO_010056
comment: Phenotype [hp:0000089] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal hypoplasia
in dataset: phenotype

Adrenal calcification [hp:0010512]
type: SIO_010056
comment: Phenotype [hp:0010512] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenal calcification
in dataset: phenotype

Abnormality of the frontal sinuses [hp:0002687]
type: SIO_010056
comment: Phenotype [hp:0002687] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the frontal sinuses
in dataset: phenotype

Hypersarcosinemia [hp:0010896]
type: SIO_010056
comment: Phenotype [hp:0010896] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypersarcosinemia
in dataset: phenotype

Generalized amyotrophy [hp:0003700]
type: SIO_010056
comment: Phenotype [hp:0003700] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized amyotrophy
in dataset: phenotype

Bifid uvula [hp:0000193]
type: SIO_010056
comment: Phenotype [hp:0000193] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid uvula
in dataset: phenotype

Hyposmia [hp:0004409]
type: SIO_010056
comment: Phenotype [hp:0004409] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyposmia
in dataset: phenotype

Epilepsia partialis continua [hp:0012847]
type: SIO_010056
comment: Phenotype [hp:0012847] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Epilepsia partialis continua
in dataset: phenotype

Congenital corneal dystrophy [hp:0008005]
type: SIO_010056
comment: Phenotype [hp:0008005] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital corneal dystrophy
in dataset: phenotype

Hypotrophy of the small hand muscles [hp:0006006]
type: SIO_010056
comment: Phenotype [hp:0006006] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypotrophy of the small hand muscles
in dataset: phenotype

Difficulty walking [hp:0002355]
type: SIO_010056
comment: Phenotype [hp:0002355] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Difficulty walking
in dataset: phenotype

Lymphedema [hp:0001004]
type: SIO_010056
comment: Phenotype [hp:0001004] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lymphedema
in dataset: phenotype

Medially deviated second toe [hp:0008096]
type: SIO_010056
comment: Phenotype [hp:0008096] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Medially deviated second toe
in dataset: phenotype

Fixed facial expression [hp:0005329]
type: SIO_010056
comment: Phenotype [hp:0005329] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fixed facial expression
in dataset: phenotype

Enlarged cisterna magna [hp:0002280]
type: SIO_010056
comment: Phenotype [hp:0002280] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged cisterna magna
in dataset: phenotype

Leukemia [hp:0001909]
type: SIO_010056
comment: Phenotype [hp:0001909] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Leukemia
in dataset: phenotype

Hypoparathyroidism [hp:0000829]
type: SIO_010056
comment: Phenotype [hp:0000829] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoparathyroidism
in dataset: phenotype

Unilateral oligodactyly [hp:0006230]
type: SIO_010056
comment: Phenotype [hp:0006230] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral oligodactyly
in dataset: phenotype

Tented upper lip vermilion [hp:0010804]
type: SIO_010056
comment: Phenotype [hp:0010804] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tented upper lip vermilion
in dataset: phenotype

Limb-girdle muscular dystrophy [hp:0006785]
type: SIO_010056
comment: Phenotype [hp:0006785] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb-girdle muscular dystrophy
in dataset: phenotype

Basal ganglia calcification [hp:0002135]
type: SIO_010056
comment: Phenotype [hp:0002135] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Basal ganglia calcification
in dataset: phenotype

Retinal flecks [hp:0012045]
type: SIO_010056
comment: Phenotype [hp:0012045] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal flecks
in dataset: phenotype

Limited knee extension [hp:0003066]
type: SIO_010056
comment: Phenotype [hp:0003066] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited knee extension
in dataset: phenotype

Monodactyly (hands) [hp:0004058]
type: SIO_010056
comment: Phenotype [hp:0004058] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Monodactyly (hands)
in dataset: phenotype

Blue cone monochromacy [hp:0007939]
type: SIO_010056
comment: Phenotype [hp:0007939] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Blue cone monochromacy
in dataset: phenotype

Narrow forehead [hp:0000341]
type: SIO_010056
comment: Phenotype [hp:0000341] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow forehead
in dataset: phenotype

Thin metacarpal cortices [hp:0006086]
type: SIO_010056
comment: Phenotype [hp:0006086] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thin metacarpal cortices
in dataset: phenotype

Renal hamartoma [hp:0008696]
type: SIO_010056
comment: Phenotype [hp:0008696] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal hamartoma
in dataset: phenotype

Ectopia pupillae [hp:0009918]
type: SIO_010056
comment: Phenotype [hp:0009918] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopia pupillae
in dataset: phenotype

Hip Subluxation [hp:0030043]
type: SIO_010056
comment: Phenotype [hp:0030043] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hip Subluxation
in dataset: phenotype

Neutropenia [hp:0001875]
type: SIO_010056
comment: Phenotype [hp:0001875] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neutropenia
in dataset: phenotype

Cough [hp:0012735]
type: SIO_010056
comment: Phenotype [hp:0012735] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cough
in dataset: phenotype

Writer's cramp [hp:0002356]
type: SIO_010056
comment: Phenotype [hp:0002356] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Writer's cramp
in dataset: phenotype

Biliary cirrhosis [hp:0002613]
type: SIO_010056
comment: Phenotype [hp:0002613] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Biliary cirrhosis
in dataset: phenotype

Abnormality of the sense of smell [hp:0004408]
type: SIO_010056
comment: Phenotype [hp:0004408] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the sense of smell
in dataset: phenotype

Xanthomatosis [hp:0000991]
type: SIO_010056
comment: Phenotype [hp:0000991] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Xanthomatosis
in dataset: phenotype

Open mouth [hp:0000194]
type: SIO_010056
comment: Phenotype [hp:0000194] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Open mouth
in dataset: phenotype

Absent vestibular function [hp:0008555]
type: SIO_010056
comment: Phenotype [hp:0008555] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent vestibular function
in dataset: phenotype

Prenatal maternal abnormality [hp:0002686]
type: SIO_010056
comment: Phenotype [hp:0002686] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prenatal maternal abnormality
in dataset: phenotype

Abolished vibration sense [hp:0006944]
type: SIO_010056
comment: Phenotype [hp:0006944] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abolished vibration sense
in dataset: phenotype

Partial fusion of tarsals [hp:0008097]
type: SIO_010056
comment: Phenotype [hp:0008097] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Partial fusion of tarsals
in dataset: phenotype

Progeroid facial appearance [hp:0005328]
type: SIO_010056
comment: Phenotype [hp:0005328] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progeroid facial appearance
in dataset: phenotype

Bony paranasal bossing [hp:0004407]
type: SIO_010056
comment: Phenotype [hp:0004407] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bony paranasal bossing
in dataset: phenotype

Patellar hypoplasia [hp:0003065]
type: SIO_010056
comment: Phenotype [hp:0003065] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Patellar hypoplasia
in dataset: phenotype

Abnormality of the basal ganglia [hp:0002134]
type: SIO_010056
comment: Phenotype [hp:0002134] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the basal ganglia
in dataset: phenotype

Retinoblastoma [hp:0009919]
type: SIO_010056
comment: Phenotype [hp:0009919] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinoblastoma
in dataset: phenotype

Paranasal sinus hypoplasia [hp:0006784]
type: SIO_010056
comment: Phenotype [hp:0006784] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paranasal sinus hypoplasia
in dataset: phenotype

Phenylpyruvic acidemia [hp:0004920]
type: SIO_010056
comment: Phenotype [hp:0004920] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Phenylpyruvic acidemia
in dataset: phenotype

Coxa magna [hp:0003279]
type: SIO_010056
comment: Phenotype [hp:0003279] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coxa magna
in dataset: phenotype

Mitten deformity [hp:0004057]
type: SIO_010056
comment: Phenotype [hp:0004057] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mitten deformity
in dataset: phenotype

Pancytopenia [hp:0001876]
type: SIO_010056
comment: Phenotype [hp:0001876] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pancytopenia
in dataset: phenotype

Self-mutilation of tongue and lips due to involuntary movements [hp:0008767]
type: SIO_010056
comment: Phenotype [hp:0008767] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Self-mutilation of tongue and lips due to involuntary movements
in dataset: phenotype

Dysphasia [hp:0002357]
type: SIO_010056
comment: Phenotype [hp:0002357] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysphasia
in dataset: phenotype

Hepatic periportal necrosis [hp:0002614]
type: SIO_010056
comment: Phenotype [hp:0002614] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatic periportal necrosis
in dataset: phenotype

Jerky ocular pursuit movements [hp:0008003]
type: SIO_010056
comment: Phenotype [hp:0008003] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Jerky ocular pursuit movements
in dataset: phenotype

Sloping forehead [hp:0000340]
type: SIO_010056
comment: Phenotype [hp:0000340] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sloping forehead
in dataset: phenotype

Hypotrichosis [hp:0001006]
type: SIO_010056
comment: Phenotype [hp:0001006] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypotrichosis
in dataset: phenotype

Cochlear malformation [hp:0008554]
type: SIO_010056
comment: Phenotype [hp:0008554] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cochlear malformation
in dataset: phenotype

Late-onset distal muscle weakness [hp:0003810]
type: SIO_010056
comment: Phenotype [hp:0003810] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Late-onset distal muscle weakness
in dataset: phenotype

Abnormality of macular pigmentation [hp:0008002]
type: SIO_010056
comment: Phenotype [hp:0008002] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of macular pigmentation
in dataset: phenotype

Severe intrauterine growth retardation [hp:0008846]
type: SIO_010056
comment: Phenotype [hp:0008846] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe intrauterine growth retardation
in dataset: phenotype

Hirsutism [hp:0001007]
type: SIO_010056
comment: Phenotype [hp:0001007] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hirsutism
in dataset: phenotype

Gastrointestinal dysmotility [hp:0002579]
type: SIO_010056
comment: Phenotype [hp:0002579] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gastrointestinal dysmotility
in dataset: phenotype

Oral cleft [hp:0000202]
type: SIO_010056
comment: Phenotype [hp:0000202] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oral cleft
in dataset: phenotype

Language impairment [hp:0002463]
type: SIO_010056
comment: Phenotype [hp:0002463] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Language impairment
in dataset: phenotype

Interphalangeal joint contracture of finger [hp:0001220]
type: SIO_010056
comment: Phenotype [hp:0001220] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Interphalangeal joint contracture of finger
in dataset: phenotype

Long philtrum [hp:0000343]
type: SIO_010056
comment: Phenotype [hp:0000343] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long philtrum
in dataset: phenotype

Abnormality of eye movement [hp:0000496]
type: SIO_010056
comment: Phenotype [hp:0000496] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of eye movement
in dataset: phenotype

Increased urinary hypoxanthine [hp:0011814]
type: SIO_010056
comment: Phenotype [hp:0011814] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased urinary hypoxanthine
in dataset: phenotype

Prolonged whole-blood clotting time [hp:0005542]
type: SIO_010056
comment: Phenotype [hp:0005542] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolonged whole-blood clotting time
in dataset: phenotype

Ankylosis of feet small joints [hp:0008090]
type: SIO_010056
comment: Phenotype [hp:0008090] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ankylosis of feet small joints
in dataset: phenotype

Intraocular melanoma [hp:0007716]
type: SIO_010056
comment: Phenotype [hp:0007716] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intraocular melanoma
in dataset: phenotype

Slender nose [hp:0000417]
type: SIO_010056
comment: Phenotype [hp:0000417] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slender nose
in dataset: phenotype

Reduced consciousness/confusion [hp:0004372]
type: SIO_010056
comment: Phenotype [hp:0004372] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced consciousness/confusion
in dataset: phenotype

Diffuse cerebral atrophy [hp:0002506]
type: SIO_010056
comment: Phenotype [hp:0002506] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse cerebral atrophy
in dataset: phenotype

Spontaneous, recurrent epistaxis [hp:0004406]
type: SIO_010056
comment: Phenotype [hp:0004406] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spontaneous, recurrent epistaxis
in dataset: phenotype

U-Shaped upper lip vermilion [hp:0010806]
type: SIO_010056
comment: Phenotype [hp:0010806] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: U-Shaped upper lip vermilion
in dataset: phenotype

Proximal femoral epiphysiolysis [hp:0006461]
type: SIO_010056
comment: Phenotype [hp:0006461] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal femoral epiphysiolysis
in dataset: phenotype

Fasting hyperinsulinemia [hp:0008283]
type: SIO_010056
comment: Phenotype [hp:0008283] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fasting hyperinsulinemia
in dataset: phenotype

Anoperineal fistula [hp:0005218]
type: SIO_010056
comment: Phenotype [hp:0005218] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anoperineal fistula
in dataset: phenotype

Short distal phalanx of the 5th finger [hp:0004227]
type: SIO_010056
comment: Phenotype [hp:0004227] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short distal phalanx of the 5th finger
in dataset: phenotype

Hypoplastic acetabulae [hp:0003274]
type: SIO_010056
comment: Phenotype [hp:0003274] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic acetabulae
in dataset: phenotype

Accumulation of melanosomes in melanocytes [hp:0001008]
type: SIO_010056
comment: Phenotype [hp:0001008] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Accumulation of melanosomes in melanocytes
in dataset: phenotype

Foveal hyperpigmentation [hp:0008001]
type: SIO_010056
comment: Phenotype [hp:0008001] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Foveal hyperpigmentation
in dataset: phenotype

Pectoralis hypoplasia [hp:0008998]
type: SIO_010056
comment: Phenotype [hp:0008998] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pectoralis hypoplasia
in dataset: phenotype

Mesomelic short stature [hp:0008845]
type: SIO_010056
comment: Phenotype [hp:0008845] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mesomelic short stature
in dataset: phenotype

Spastic dysarthria [hp:0002464]
type: SIO_010056
comment: Phenotype [hp:0002464] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spastic dysarthria
in dataset: phenotype

Rhizomelia [hp:0008905]
type: SIO_010056
comment: Phenotype [hp:0008905] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rhizomelia
in dataset: phenotype

Gastroparesis [hp:0002578]
type: SIO_010056
comment: Phenotype [hp:0002578] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gastroparesis
in dataset: phenotype

Oromotor apraxia [hp:0007301]
type: SIO_010056
comment: Phenotype [hp:0007301] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oromotor apraxia
in dataset: phenotype

Microphthalmos [hp:0000568]
type: SIO_010056
comment: Phenotype [hp:0000568] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microphthalmos
in dataset: phenotype

Pierre-Robin sequence [hp:0000201]
type: SIO_010056
comment: Phenotype [hp:0000201] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pierre-Robin sequence
in dataset: phenotype

Neoplasia of the nasopharynx [hp:0100630]
type: SIO_010056
comment: Phenotype [hp:0100630] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasia of the nasopharynx
in dataset: phenotype

Clusters of axonal regeneration [hp:0007233]
type: SIO_010056
comment: Phenotype [hp:0007233] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Clusters of axonal regeneration
in dataset: phenotype

Recurrent corneal erosions [hp:0000495]
type: SIO_010056
comment: Phenotype [hp:0000495] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent corneal erosions
in dataset: phenotype

Exercise-induced muscle fatigue [hp:0009020]
type: SIO_010056
comment: Phenotype [hp:0009020] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exercise-induced muscle fatigue
in dataset: phenotype

Decreased/absent ankle reflexes [hp:0200101]
type: SIO_010056
comment: Phenotype [hp:0200101] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased/absent ankle reflexes
in dataset: phenotype

Recurrent Neisserial infections [hp:0005430]
type: SIO_010056
comment: Phenotype [hp:0005430] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent Neisserial infections
in dataset: phenotype

Reduced protein C activity [hp:0005543]
type: SIO_010056
comment: Phenotype [hp:0005543] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced protein C activity
in dataset: phenotype

Nodular corneal dystrophy [hp:0007827]
type: SIO_010056
comment: Phenotype [hp:0007827] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nodular corneal dystrophy
in dataset: phenotype

Progressive muscle weakness [hp:0003323]
type: SIO_010056
comment: Phenotype [hp:0003323] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive muscle weakness
in dataset: phenotype

Polysyndactyly of hallux [hp:0005873]
type: SIO_010056
comment: Phenotype [hp:0005873] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polysyndactyly of hallux
in dataset: phenotype

Short proximal phalanx of hallux [hp:0010107]
type: SIO_010056
comment: Phenotype [hp:0010107] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short proximal phalanx of hallux
in dataset: phenotype

Focal dystonia [hp:0004373]
type: SIO_010056
comment: Phenotype [hp:0004373] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Focal dystonia
in dataset: phenotype

Alopecia universalis [hp:0002289]
type: SIO_010056
comment: Phenotype [hp:0002289] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Alopecia universalis
in dataset: phenotype

Narrow nasal ridge [hp:0000418]
type: SIO_010056
comment: Phenotype [hp:0000418] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow nasal ridge
in dataset: phenotype

Reduced systolic function [hp:0006673]
type: SIO_010056
comment: Phenotype [hp:0006673] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced systolic function
in dataset: phenotype

Open bite [hp:0010807]
type: SIO_010056
comment: Phenotype [hp:0010807] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Open bite
in dataset: phenotype

Duplication of internal organs [hp:0005217]
type: SIO_010056
comment: Phenotype [hp:0005217] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Duplication of internal organs
in dataset: phenotype

Facial tics [hp:0011468]
type: SIO_010056
comment: Phenotype [hp:0011468] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial tics
in dataset: phenotype

Semilobar holoprosencephaly [hp:0002507]
type: SIO_010056
comment: Phenotype [hp:0002507] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Semilobar holoprosencephaly
in dataset: phenotype

Generalized bone demineralization [hp:0006462]
type: SIO_010056
comment: Phenotype [hp:0006462] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized bone demineralization
in dataset: phenotype

Hip contracture [hp:0003273]
type: SIO_010056
comment: Phenotype [hp:0003273] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hip contracture
in dataset: phenotype

Prominent nipples [hp:0004405]
type: SIO_010056
comment: Phenotype [hp:0004405] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent nipples
in dataset: phenotype

Unconjugated hyperbilirubinemia [hp:0008282]
type: SIO_010056
comment: Phenotype [hp:0008282] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unconjugated hyperbilirubinemia
in dataset: phenotype

Poor speech [hp:0002465]
type: SIO_010056
comment: Phenotype [hp:0002465] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poor speech
in dataset: phenotype

Bilateral vestibular Schwannoma [hp:0009589]
type: SIO_010056
comment: Phenotype [hp:0009589] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral vestibular Schwannoma
in dataset: phenotype

Episodic peripheral neuropathy [hp:0006949]
type: SIO_010056
comment: Phenotype [hp:0006949] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic peripheral neuropathy
in dataset: phenotype

Abnormality of oral frenula [hp:0000190]
type: SIO_010056
comment: Phenotype [hp:0000190] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of oral frenula
in dataset: phenotype

Calcification of the small brain vessels [hp:0002504]
type: SIO_010056
comment: Phenotype [hp:0002504] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcification of the small brain vessels
in dataset: phenotype

Reduced von Willebrand factor activity [hp:0008330]
type: SIO_010056
comment: Phenotype [hp:0008330] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced von Willebrand factor activity
in dataset: phenotype

Abnormality of the stomach [hp:0002577]
type: SIO_010056
comment: Phenotype [hp:0002577] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the stomach
in dataset: phenotype

Decreased corneal reflex [hp:0008000]
type: SIO_010056
comment: Phenotype [hp:0008000] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased corneal reflex
in dataset: phenotype

Proximal muscle weakness in upper limbs [hp:0008997]
type: SIO_010056
comment: Phenotype [hp:0008997] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal muscle weakness in upper limbs
in dataset: phenotype

Blepharitis [hp:0000498]
type: SIO_010056
comment: Phenotype [hp:0000498] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Blepharitis
in dataset: phenotype

Ectopic posterior pituitary [hp:0011755]
type: SIO_010056
comment: Phenotype [hp:0011755] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopic posterior pituitary
in dataset: phenotype

Recurrent subcortical infarcts [hp:0007236]
type: SIO_010056
comment: Phenotype [hp:0007236] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent subcortical infarcts
in dataset: phenotype

Cleft upper lip [hp:0000204]
type: SIO_010056
comment: Phenotype [hp:0000204] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cleft upper lip
in dataset: phenotype

Protruding tongue [hp:0010808]
type: SIO_010056
comment: Phenotype [hp:0010808] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Protruding tongue
in dataset: phenotype

Abnormality of temperature regulation [hp:0004370]
type: SIO_010056
comment: Phenotype [hp:0004370] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of temperature regulation
in dataset: phenotype

Generalized muscle weakness [hp:0003324]
type: SIO_010056
comment: Phenotype [hp:0003324] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized muscle weakness
in dataset: phenotype

Brachytelomesophalangy [hp:0005872]
type: SIO_010056
comment: Phenotype [hp:0005872] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Brachytelomesophalangy
in dataset: phenotype

Sparse or absent eyelashes [hp:0200102]
type: SIO_010056
comment: Phenotype [hp:0200102] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sparse or absent eyelashes
in dataset: phenotype

Rhinitis [hp:0012384]
type: SIO_010056
comment: Phenotype [hp:0012384] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rhinitis
in dataset: phenotype

Fusion of the cerebellar hemispheres [hp:0006899]
type: SIO_010056
comment: Phenotype [hp:0006899] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fusion of the cerebellar hemispheres
in dataset: phenotype

Telangiectasia [hp:0001009]
type: SIO_010056
comment: Phenotype [hp:0001009] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Telangiectasia
in dataset: phenotype

Pelvic exostoses [hp:0003276]
type: SIO_010056
comment: Phenotype [hp:0003276] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pelvic exostoses
in dataset: phenotype

Lactic acidosis [hp:0003128]
type: SIO_010056
comment: Phenotype [hp:0003128] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lactic acidosis
in dataset: phenotype

Craniofacial dysostosis [hp:0004439]
type: SIO_010056
comment: Phenotype [hp:0004439] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Craniofacial dysostosis
in dataset: phenotype

Absent gallbladder [hp:0011467]
type: SIO_010056
comment: Phenotype [hp:0011467] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent gallbladder
in dataset: phenotype

Abnormality of the nipple [hp:0004404]
type: SIO_010056
comment: Phenotype [hp:0004404] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the nipple
in dataset: phenotype

Mitochondrial encephalopathy [hp:0006789]
type: SIO_010056
comment: Phenotype [hp:0006789] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mitochondrial encephalopathy
in dataset: phenotype

Acute hyperammonemia [hp:0008281]
type: SIO_010056
comment: Phenotype [hp:0008281] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute hyperammonemia
in dataset: phenotype

Medial flaring of the eyebrow [hp:0010747]
type: SIO_010056
comment: Phenotype [hp:0010747] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Medial flaring of the eyebrow
in dataset: phenotype

Accessory oral frenulum [hp:0000191]
type: SIO_010056
comment: Phenotype [hp:0000191] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Accessory oral frenulum
in dataset: phenotype

Absent paranasal sinuses [hp:0002689]
type: SIO_010056
comment: Phenotype [hp:0002689] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent paranasal sinuses
in dataset: phenotype

Vestibular Schwannoma [hp:0009588]
type: SIO_010056
comment: Phenotype [hp:0009588] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vestibular Schwannoma
in dataset: phenotype

Intussusception [hp:0002576]
type: SIO_010056
comment: Phenotype [hp:0002576] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intussusception
in dataset: phenotype

Hip osteoarthritis [hp:0008843]
type: SIO_010056
comment: Phenotype [hp:0008843] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hip osteoarthritis
in dataset: phenotype

Diffuse retinal cone degeneration [hp:0007829]
type: SIO_010056
comment: Phenotype [hp:0007829] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse retinal cone degeneration
in dataset: phenotype

Infantile sensorineural hearing impairment [hp:0008610]
type: SIO_010056
comment: Phenotype [hp:0008610] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Infantile sensorineural hearing impairment
in dataset: phenotype

Tibial deviation of toes [hp:0100499]
type: SIO_010056
comment: Phenotype [hp:0100499] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tibial deviation of toes
in dataset: phenotype

Common atrium [hp:0011565]
type: SIO_010056
comment: Phenotype [hp:0011565] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Common atrium
in dataset: phenotype

Short hallux [hp:0010109]
type: SIO_010056
comment: Phenotype [hp:0010109] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short hallux
in dataset: phenotype

Metaphyseal chondrodysplasia [hp:0005871]
type: SIO_010056
comment: Phenotype [hp:0005871] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metaphyseal chondrodysplasia
in dataset: phenotype

Limb-girdle muscle weakness [hp:0003325]
type: SIO_010056
comment: Phenotype [hp:0003325] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb-girdle muscle weakness
in dataset: phenotype

Congenital agranulocytosis [hp:0005541]
type: SIO_010056
comment: Phenotype [hp:0005541] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital agranulocytosis
in dataset: phenotype

Narrow pelvis [hp:0003275]
type: SIO_010056
comment: Phenotype [hp:0003275] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow pelvis
in dataset: phenotype

Absence of intrinsic factor [hp:0005219]
type: SIO_010056
comment: Phenotype [hp:0005219] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of intrinsic factor
in dataset: phenotype

Increased laxity of ankles [hp:0006460]
type: SIO_010056
comment: Phenotype [hp:0006460] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased laxity of ankles
in dataset: phenotype

Short 4th toe [hp:0008093]
type: SIO_010056
comment: Phenotype [hp:0008093] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short 4th toe
in dataset: phenotype

Progressive inability to walk [hp:0002505]
type: SIO_010056
comment: Phenotype [hp:0002505] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive inability to walk
in dataset: phenotype

Micrognathia [hp:0000347]
type: SIO_010056
comment: Phenotype [hp:0000347] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Micrognathia
in dataset: phenotype

Esophagitis [hp:0100633]
type: SIO_010056
comment: Phenotype [hp:0100633] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Esophagitis
in dataset: phenotype

Absent first metatarsal [hp:0010104]
type: SIO_010056
comment: Phenotype [hp:0010104] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent first metatarsal
in dataset: phenotype

Atresia of the external auditory canal [hp:0000413]
type: SIO_010056
comment: Phenotype [hp:0000413] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atresia of the external auditory canal
in dataset: phenotype

Decreased distal sensory nerve action potential [hp:0007230]
type: SIO_010056
comment: Phenotype [hp:0007230] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased distal sensory nerve action potential
in dataset: phenotype

Reduced erythrocyte 2,3-diphosphoglycerate concentration [hp:0030271]
type: SIO_010056
comment: Phenotype [hp:0030271] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced erythrocyte 2,3-diphosphoglycerate concentration
in dataset: phenotype

Abnormality of the eyelid [hp:0000492]
type: SIO_010056
comment: Phenotype [hp:0000492] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the eyelid
in dataset: phenotype

Aplasia/Hypoplasia of the distal phalanges of the toes [hp:0010185]
type: SIO_010056
comment: Phenotype [hp:0010185] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the distal phalanges of the toes
in dataset: phenotype

Tracheoesophageal fistula [hp:0002575]
type: SIO_010056
comment: Phenotype [hp:0002575] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tracheoesophageal fistula
in dataset: phenotype

Mitral atresia [hp:0011560]
type: SIO_010056
comment: Phenotype [hp:0011560] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mitral atresia
in dataset: phenotype

Edema of the lower limbs [hp:0010741]
type: SIO_010056
comment: Phenotype [hp:0010741] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Edema of the lower limbs
in dataset: phenotype

Complex organic aciduria [hp:0008336]
type: SIO_010056
comment: Phenotype [hp:0008336] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Complex organic aciduria
in dataset: phenotype

Keratoglobus [hp:0001119]
type: SIO_010056
comment: Phenotype [hp:0001119] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Keratoglobus
in dataset: phenotype

Intestinal obstruction [hp:0005214]
type: SIO_010056
comment: Phenotype [hp:0005214] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intestinal obstruction
in dataset: phenotype

Fair hair [hp:0002286]
type: SIO_010056
comment: Phenotype [hp:0002286] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fair hair
in dataset: phenotype

Abdominal distention [hp:0003270]
type: SIO_010056
comment: Phenotype [hp:0003270] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abdominal distention
in dataset: phenotype

Interosseus muscle atrophy [hp:0007181]
type: SIO_010056
comment: Phenotype [hp:0007181] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Interosseus muscle atrophy
in dataset: phenotype

Cranial hyperostosis [hp:0004437]
type: SIO_010056
comment: Phenotype [hp:0004437] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cranial hyperostosis
in dataset: phenotype

Increased red cell osmotic resistance [hp:0005546]
type: SIO_010056
comment: Phenotype [hp:0005546] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased red cell osmotic resistance
in dataset: phenotype

Cranial nerve VI palsy [hp:0006897]
type: SIO_010056
comment: Phenotype [hp:0006897] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cranial nerve VI palsy
in dataset: phenotype

Impaired myocardial contractility [hp:0006670]
type: SIO_010056
comment: Phenotype [hp:0006670] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired myocardial contractility
in dataset: phenotype

Type II transferrin isoform profile [hp:0012301]
type: SIO_010056
comment: Phenotype [hp:0012301] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type II transferrin isoform profile
in dataset: phenotype

Hemophagocytosis [hp:0012156]
type: SIO_010056
comment: Phenotype [hp:0012156] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemophagocytosis
in dataset: phenotype

Aortic dilatation [hp:0001724]
type: SIO_010056
comment: Phenotype [hp:0001724] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aortic dilatation
in dataset: phenotype

Myalgia [hp:0003326]
type: SIO_010056
comment: Phenotype [hp:0003326] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myalgia
in dataset: phenotype

Neuroendocrine neoplasm [hp:0100634]
type: SIO_010056
comment: Phenotype [hp:0100634] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neuroendocrine neoplasm
in dataset: phenotype

Bulbous nose [hp:0000414]
type: SIO_010056
comment: Phenotype [hp:0000414] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bulbous nose
in dataset: phenotype

Whistling appearance [hp:0000346]
type: SIO_010056
comment: Phenotype [hp:0000346] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Whistling appearance
in dataset: phenotype

Elevated red cell adenosine deaminase activity [hp:0030270]
type: SIO_010056
comment: Phenotype [hp:0030270] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated red cell adenosine deaminase activity
in dataset: phenotype

Proximal muscle weakness in lower limbs [hp:0008994]
type: SIO_010056
comment: Phenotype [hp:0008994] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal muscle weakness in lower limbs
in dataset: phenotype

Duplicated collecting system [hp:0000081]
type: SIO_010056
comment: Phenotype [hp:0000081] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Duplicated collecting system
in dataset: phenotype

Triangular epiphysis of the proximal phalanx of the 3rd finger [hp:0009356]
type: SIO_010056
comment: Phenotype [hp:0009356] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular epiphysis of the proximal phalanx of the 3rd finger
in dataset: phenotype

Abnormal respiratory motile cilium morphology [hp:0005938]
type: SIO_010056
comment: Phenotype [hp:0005938] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal respiratory motile cilium morphology
in dataset: phenotype

Episodic abdominal pain [hp:0002574]
type: SIO_010056
comment: Phenotype [hp:0002574] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic abdominal pain
in dataset: phenotype

Pointed proximal second through fifth metacarpals [hp:0001223]
type: SIO_010056
comment: Phenotype [hp:0001223] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pointed proximal second through fifth metacarpals
in dataset: phenotype

Keratitis [hp:0000491]
type: SIO_010056
comment: Phenotype [hp:0000491] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Keratitis
in dataset: phenotype

Juvenile cataract [hp:0001118]
type: SIO_010056
comment: Phenotype [hp:0001118] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Juvenile cataract
in dataset: phenotype

CNS demyelination [hp:0007305]
type: SIO_010056
comment: Phenotype [hp:0007305] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: CNS demyelination
in dataset: phenotype

Depletion of mitochondrial DNA in muscle tissue [hp:0009141]
type: SIO_010056
comment: Phenotype [hp:0009141] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Depletion of mitochondrial DNA in muscle tissue
in dataset: phenotype

Submucous cleft soft palate [hp:0011819]
type: SIO_010056
comment: Phenotype [hp:0011819] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Submucous cleft soft palate
in dataset: phenotype

Peripheral hypomyelination [hp:0007182]
type: SIO_010056
comment: Phenotype [hp:0007182] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral hypomyelination
in dataset: phenotype

Myeloproliferative disorder [hp:0005547]
type: SIO_010056
comment: Phenotype [hp:0005547] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myeloproliferative disorder
in dataset: phenotype

Hyperostosis frontalis interna [hp:0004438]
type: SIO_010056
comment: Phenotype [hp:0004438] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperostosis frontalis interna
in dataset: phenotype

Meconium ileus [hp:0004401]
type: SIO_010056
comment: Phenotype [hp:0004401] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Meconium ileus
in dataset: phenotype

Fetal megacystis [hp:0010956]
type: SIO_010056
comment: Phenotype [hp:0010956] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fetal megacystis
in dataset: phenotype

Hematological neoplasm [hp:0004377]
type: SIO_010056
comment: Phenotype [hp:0004377] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hematological neoplasm
in dataset: phenotype

Herpes simplex encephalitis [hp:0012302]
type: SIO_010056
comment: Phenotype [hp:0012302] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Herpes simplex encephalitis
in dataset: phenotype

Axial muscle weakness [hp:0003327]
type: SIO_010056
comment: Phenotype [hp:0003327] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Axial muscle weakness
in dataset: phenotype

Transposition of the great arteries [hp:0001669]
type: SIO_010056
comment: Phenotype [hp:0001669] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Transposition of the great arteries
in dataset: phenotype

Pancreatic calcification [hp:0005213]
type: SIO_010056
comment: Phenotype [hp:0005213] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pancreatic calcification
in dataset: phenotype

Spinocerebellar tract disease in lower limbs [hp:0007232]
type: SIO_010056
comment: Phenotype [hp:0007232] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinocerebellar tract disease in lower limbs
in dataset: phenotype

Aplasia cutis congenita of scalp [hp:0007385]
type: SIO_010056
comment: Phenotype [hp:0007385] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia cutis congenita of scalp
in dataset: phenotype

Increased serum free triiodothyronine (fT3) [hp:0011788]
type: SIO_010056
comment: Phenotype [hp:0011788] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased serum free triiodothyronine (fT3)
in dataset: phenotype

Short lingual frenulum [hp:0000200]
type: SIO_010056
comment: Phenotype [hp:0000200] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short lingual frenulum
in dataset: phenotype

Hematochezia [hp:0002573]
type: SIO_010056
comment: Phenotype [hp:0002573] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hematochezia
in dataset: phenotype

Neoplasm of the adrenal gland [hp:0100631]
type: SIO_010056
comment: Phenotype [hp:0100631] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the adrenal gland
in dataset: phenotype

Increased intraabdominal fat [hp:0008993]
type: SIO_010056
comment: Phenotype [hp:0008993] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased intraabdominal fat
in dataset: phenotype

Protruding ear [hp:0000411]
type: SIO_010056
comment: Phenotype [hp:0000411] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Protruding ear
in dataset: phenotype

High-output congestive heart failure [hp:0001722]
type: SIO_010056
comment: Phenotype [hp:0001722] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High-output congestive heart failure
in dataset: phenotype

Bipolar affective disorder [hp:0007302]
type: SIO_010056
comment: Phenotype [hp:0007302] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bipolar affective disorder
in dataset: phenotype

Moderately short stature [hp:0008848]
type: SIO_010056
comment: Phenotype [hp:0008848] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Moderately short stature
in dataset: phenotype

Short metatarsal [hp:0010743]
type: SIO_010056
comment: Phenotype [hp:0010743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short metatarsal
in dataset: phenotype

Severe photosensitivity [hp:0007537]
type: SIO_010056
comment: Phenotype [hp:0007537] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe photosensitivity
in dataset: phenotype

Reduced red cell adenosine deaminase activity [hp:0030273]
type: SIO_010056
comment: Phenotype [hp:0030273] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced red cell adenosine deaminase activity
in dataset: phenotype

Downslanted palpebral fissures [hp:0000494]
type: SIO_010056
comment: Phenotype [hp:0000494] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Downslanted palpebral fissures
in dataset: phenotype

Spatulate thumbs [hp:0001222]
type: SIO_010056
comment: Phenotype [hp:0001222] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spatulate thumbs
in dataset: phenotype

Abnormality of reproductive system physiology [hp:0000080]
type: SIO_010056
comment: Phenotype [hp:0000080] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of reproductive system physiology
in dataset: phenotype

Childhood onset [hp:0011463]
type: SIO_010056
comment: Phenotype [hp:0011463] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Childhood onset
in dataset: phenotype

Abnormality of the hip bone [hp:0003272]
type: SIO_010056
comment: Phenotype [hp:0003272] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the hip bone
in dataset: phenotype

Predominantly lower limb lymphedema [hp:0003550]
type: SIO_010056
comment: Phenotype [hp:0003550] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Predominantly lower limb lymphedema
in dataset: phenotype

Chewing difficulties [hp:0005216]
type: SIO_010056
comment: Phenotype [hp:0005216] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chewing difficulties
in dataset: phenotype

Congenital posterior urethral valve [hp:0010957]
type: SIO_010056
comment: Phenotype [hp:0010957] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital posterior urethral valve
in dataset: phenotype

Brainstem dysplasia [hp:0002508]
type: SIO_010056
comment: Phenotype [hp:0002508] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Brainstem dysplasia
in dataset: phenotype

Mandibulofacial dysostosis [hp:0005321]
type: SIO_010056
comment: Phenotype [hp:0005321] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mandibulofacial dysostosis
in dataset: phenotype

Widow's peak [hp:0000349]
type: SIO_010056
comment: Phenotype [hp:0000349] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Widow's peak
in dataset: phenotype

Hemiplegia/hemiparesis [hp:0004374]
type: SIO_010056
comment: Phenotype [hp:0004374] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemiplegia/hemiparesis
in dataset: phenotype

Lower limb hypertonia [hp:0006895]
type: SIO_010056
comment: Phenotype [hp:0006895] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lower limb hypertonia
in dataset: phenotype

Episodic vomiting [hp:0002572]
type: SIO_010056
comment: Phenotype [hp:0002572] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic vomiting
in dataset: phenotype

Central hypothyroidism [hp:0011787]
type: SIO_010056
comment: Phenotype [hp:0011787] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Central hypothyroidism
in dataset: phenotype

Aberrant melanosome maturation [hp:0007384]
type: SIO_010056
comment: Phenotype [hp:0007384] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aberrant melanosome maturation
in dataset: phenotype

Short first metatarsal [hp:0010105]
type: SIO_010056
comment: Phenotype [hp:0010105] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short first metatarsal
in dataset: phenotype

Restrictive cardiomyopathy [hp:0001723]
type: SIO_010056
comment: Phenotype [hp:0001723] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Restrictive cardiomyopathy
in dataset: phenotype

High forehead [hp:0000348]
type: SIO_010056
comment: Phenotype [hp:0000348] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High forehead
in dataset: phenotype

Radial deviation of the 2nd finger [hp:0009467]
type: SIO_010056
comment: Phenotype [hp:0009467] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Radial deviation of the 2nd finger
in dataset: phenotype

Macular coloboma [hp:0001116]
type: SIO_010056
comment: Phenotype [hp:0001116] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macular coloboma
in dataset: phenotype

Hypoplastic radial head [hp:0003997]
type: SIO_010056
comment: Phenotype [hp:0003997] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic radial head
in dataset: phenotype

Renal aminoaciduria [hp:0008335]
type: SIO_010056
comment: Phenotype [hp:0008335] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal aminoaciduria
in dataset: phenotype

Abnormality of the fovea [hp:0000493]
type: SIO_010056
comment: Phenotype [hp:0000493] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the fovea
in dataset: phenotype

Multinucleated giant chondrocytes in epiphyseal cartilage [hp:0030330]
type: SIO_010056
comment: Phenotype [hp:0030330] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multinucleated giant chondrocytes in epiphyseal cartilage
in dataset: phenotype

Young adult onset [hp:0011462]
type: SIO_010056
comment: Phenotype [hp:0011462] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Young adult onset
in dataset: phenotype

Limb hypertonia [hp:0002509]
type: SIO_010056
comment: Phenotype [hp:0002509] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb hypertonia
in dataset: phenotype

Difficulty climbing stairs [hp:0003551]
type: SIO_010056
comment: Phenotype [hp:0003551] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Difficulty climbing stairs
in dataset: phenotype

Visceromegaly [hp:0003271]
type: SIO_010056
comment: Phenotype [hp:0003271] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Visceromegaly
in dataset: phenotype

Absent metatarsal bone [hp:0010744]
type: SIO_010056
comment: Phenotype [hp:0010744] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent metatarsal bone
in dataset: phenotype

Frequent Giardia lamblia infestation [hp:0005215]
type: SIO_010056
comment: Phenotype [hp:0005215] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frequent Giardia lamblia infestation
in dataset: phenotype

Progressive alopecia [hp:0002287]
type: SIO_010056
comment: Phenotype [hp:0002287] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive alopecia
in dataset: phenotype

Retinal vascular tortuosity [hp:0012841]
type: SIO_010056
comment: Phenotype [hp:0012841] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal vascular tortuosity
in dataset: phenotype

Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes [hp:0003329]
type: SIO_010056
comment: Phenotype [hp:0003329] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes
in dataset: phenotype

Paroxysmal atrial tachycardia [hp:0006671]
type: SIO_010056
comment: Phenotype [hp:0006671] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paroxysmal atrial tachycardia
in dataset: phenotype

Congenital localized absence of skin [hp:0007383]
type: SIO_010056
comment: Phenotype [hp:0007383] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital localized absence of skin
in dataset: phenotype

Hypnopompic hallucinations [hp:0006896]
type: SIO_010056
comment: Phenotype [hp:0006896] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypnopompic hallucinations
in dataset: phenotype

Neoplasm of the nervous system [hp:0004375]
type: SIO_010056
comment: Phenotype [hp:0004375] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the nervous system
in dataset: phenotype

Limb pain [hp:0009763]
type: SIO_010056
comment: Phenotype [hp:0009763] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb pain
in dataset: phenotype

Hypoplasia of olfactory tract [hp:0007036]
type: SIO_010056
comment: Phenotype [hp:0007036] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of olfactory tract
in dataset: phenotype

Leukodystrophy [hp:0002415]
type: SIO_010056
comment: Phenotype [hp:0002415] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Leukodystrophy
in dataset: phenotype

Mastocytosis [hp:0100495]
type: SIO_010056
comment: Phenotype [hp:0100495] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mastocytosis
in dataset: phenotype

Thick anterior alveolar ridges [hp:0009100]
type: SIO_010056
comment: Phenotype [hp:0009100] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thick anterior alveolar ridges
in dataset: phenotype

Nephrogenic diabetes insipidus [hp:0009806]
type: SIO_010056
comment: Phenotype [hp:0009806] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nephrogenic diabetes insipidus
in dataset: phenotype

Sudden death [hp:0001699]
type: SIO_010056
comment: Phenotype [hp:0001699] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sudden death
in dataset: phenotype

Contiguous gene syndrome [hp:0001466]
type: SIO_010056
comment: Phenotype [hp:0001466] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Contiguous gene syndrome
in dataset: phenotype

Tics [hp:0100033]
type: SIO_010056
comment: Phenotype [hp:0100033] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tics
in dataset: phenotype

Acral ulceration leading to autoamputation of digits [hp:0006121]
type: SIO_010056
comment: Phenotype [hp:0006121] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acral ulceration leading to autoamputation of digits
in dataset: phenotype

Diabetic ketoacidosis [hp:0001953]
type: SIO_010056
comment: Phenotype [hp:0001953] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diabetic ketoacidosis
in dataset: phenotype

Leydig cell insensitivity to gonadotropin [hp:0002929]
type: SIO_010056
comment: Phenotype [hp:0002929] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Leydig cell insensitivity to gonadotropin
in dataset: phenotype

Dysphonia [hp:0001618]
type: SIO_010056
comment: Phenotype [hp:0001618] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysphonia
in dataset: phenotype

Elevated urinary norepinephrine [hp:0003345]
type: SIO_010056
comment: Phenotype [hp:0003345] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated urinary norepinephrine
in dataset: phenotype

Muscle hyperirritability [hp:0003559]
type: SIO_010056
comment: Phenotype [hp:0003559] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscle hyperirritability
in dataset: phenotype

Shallow acetabular fossae [hp:0003182]
type: SIO_010056
comment: Phenotype [hp:0003182] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shallow acetabular fossae
in dataset: phenotype

Abnormality of the middle ear ossicles [hp:0004452]
type: SIO_010056
comment: Phenotype [hp:0004452] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the middle ear ossicles
in dataset: phenotype

Opacification of the corneal stroma [hp:0007759]
type: SIO_010056
comment: Phenotype [hp:0007759] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Opacification of the corneal stroma
in dataset: phenotype

Duodenal atresia [hp:0002247]
type: SIO_010056
comment: Phenotype [hp:0002247] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Duodenal atresia
in dataset: phenotype

Esophageal diverticulum [hp:0100628]
type: SIO_010056
comment: Phenotype [hp:0100628] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Esophageal diverticulum
in dataset: phenotype

Congenital ptosis [hp:0007970]
type: SIO_010056
comment: Phenotype [hp:0007970] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital ptosis
in dataset: phenotype

Short 1st metacarpal [hp:0010034]
type: SIO_010056
comment: Phenotype [hp:0010034] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short 1st metacarpal
in dataset: phenotype

Proximal fibular overgrowth [hp:0005067]
type: SIO_010056
comment: Phenotype [hp:0005067] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal fibular overgrowth
in dataset: phenotype

Motor tics [hp:0100034]
type: SIO_010056
comment: Phenotype [hp:0100034] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Motor tics
in dataset: phenotype

Lumbar kyphosis in infancy [hp:0008414]
type: SIO_010056
comment: Phenotype [hp:0008414] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lumbar kyphosis in infancy
in dataset: phenotype

Subependymal cysts [hp:0002416]
type: SIO_010056
comment: Phenotype [hp:0002416] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subependymal cysts
in dataset: phenotype

Impaired visuospatial constructive cognition [hp:0010794]
type: SIO_010056
comment: Phenotype [hp:0010794] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired visuospatial constructive cognition
in dataset: phenotype

Facial wrinkling [hp:0009762]
type: SIO_010056
comment: Phenotype [hp:0009762] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial wrinkling
in dataset: phenotype

Anterior encephalocele [hp:0007035]
type: SIO_010056
comment: Phenotype [hp:0007035] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior encephalocele
in dataset: phenotype

Submucous cleft lip [hp:0009101]
type: SIO_010056
comment: Phenotype [hp:0009101] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Submucous cleft lip
in dataset: phenotype

Giant somatosensory evoked potentials [hp:0001312]
type: SIO_010056
comment: Phenotype [hp:0001312] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Giant somatosensory evoked potentials
in dataset: phenotype

Abnormal iron deposition in mitochondria [hp:0008306]
type: SIO_010056
comment: Phenotype [hp:0008306] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal iron deposition in mitochondria
in dataset: phenotype

Somnolence [hp:0001262]
type: SIO_010056
comment: Phenotype [hp:0001262] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Somnolence
in dataset: phenotype

Nasolacrimal duct obstruction [hp:0000579]
type: SIO_010056
comment: Phenotype [hp:0000579] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nasolacrimal duct obstruction
in dataset: phenotype

Abnormal glucose tolerance [hp:0001952]
type: SIO_010056
comment: Phenotype [hp:0001952] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal glucose tolerance
in dataset: phenotype

Congenital visual impairment [hp:0007758]
type: SIO_010056
comment: Phenotype [hp:0007758] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital visual impairment
in dataset: phenotype

Wide pubic symphysis [hp:0003183]
type: SIO_010056
comment: Phenotype [hp:0003183] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Wide pubic symphysis
in dataset: phenotype

Hematemesis [hp:0002248]
type: SIO_010056
comment: Phenotype [hp:0002248] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hematemesis
in dataset: phenotype

3-Methylglutaric aciduria [hp:0003344]
type: SIO_010056
comment: Phenotype [hp:0003344] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 3-Methylglutaric aciduria
in dataset: phenotype

High, narrow palate [hp:0002705]
type: SIO_010056
comment: Phenotype [hp:0002705] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High, narrow palate
in dataset: phenotype

Viral infection-induced rhabdomyolysis [hp:0003558]
type: SIO_010056
comment: Phenotype [hp:0003558] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Viral infection-induced rhabdomyolysis
in dataset: phenotype

Decreased activity of the pyruvate dehydrogenase (PDH) complex [hp:0002928]
type: SIO_010056
comment: Phenotype [hp:0002928] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased activity of the pyruvate dehydrogenase (PDH) complex
in dataset: phenotype

Concave nasal ridge [hp:0011120]
type: SIO_010056
comment: Phenotype [hp:0011120] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Concave nasal ridge
in dataset: phenotype

Displacement of the external urethral meatus [hp:0100627]
type: SIO_010056
comment: Phenotype [hp:0100627] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Displacement of the external urethral meatus
in dataset: phenotype

Postauricular skin tag [hp:0004451]
type: SIO_010056
comment: Phenotype [hp:0004451] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Postauricular skin tag
in dataset: phenotype

Slender long bone [hp:0003100]
type: SIO_010056
comment: Phenotype [hp:0003100] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slender long bone
in dataset: phenotype

Lamellar cataract [hp:0007971]
type: SIO_010056
comment: Phenotype [hp:0007971] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lamellar cataract
in dataset: phenotype

Pontocerebellar atrophy [hp:0006879]
type: SIO_010056
comment: Phenotype [hp:0006879] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pontocerebellar atrophy
in dataset: phenotype

Proximal tibial hypopolasia [hp:0006379]
type: SIO_010056
comment: Phenotype [hp:0006379] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal tibial hypopolasia
in dataset: phenotype

Absent styloid process of ulna [hp:0005068]
type: SIO_010056
comment: Phenotype [hp:0005068] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent styloid process of ulna
in dataset: phenotype

Pseudoepiphyses of the metacarpals [hp:0009193]
type: SIO_010056
comment: Phenotype [hp:0009193] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pseudoepiphyses of the metacarpals
in dataset: phenotype

Dry skin [hp:0000958]
type: SIO_010056
comment: Phenotype [hp:0000958] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dry skin
in dataset: phenotype

Anterior open-bite malocclusion [hp:0009102]
type: SIO_010056
comment: Phenotype [hp:0009102] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior open-bite malocclusion
in dataset: phenotype

Low hanging columella [hp:0009765]
type: SIO_010056
comment: Phenotype [hp:0009765] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low hanging columella
in dataset: phenotype

Hypoammonemia [hp:0100493]
type: SIO_010056
comment: Phenotype [hp:0100493] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoammonemia
in dataset: phenotype

Phonic tics [hp:0100035]
type: SIO_010056
comment: Phenotype [hp:0100035] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Phonic tics
in dataset: phenotype

Centrocecal scotoma [hp:0000576]
type: SIO_010056
comment: Phenotype [hp:0000576] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Centrocecal scotoma
in dataset: phenotype

Global developmental delay [hp:0001263]
type: SIO_010056
comment: Phenotype [hp:0001263] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Global developmental delay
in dataset: phenotype

Abnormality of the pericardium [hp:0001697]
type: SIO_010056
comment: Phenotype [hp:0001697] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the pericardium
in dataset: phenotype

Reduced number of teeth [hp:0009804]
type: SIO_010056
comment: Phenotype [hp:0009804] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced number of teeth
in dataset: phenotype

Medium chain dicarboxylic aciduria [hp:0008309]
type: SIO_010056
comment: Phenotype [hp:0008309] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Medium chain dicarboxylic aciduria
in dataset: phenotype

Abnormal nervous system electrophysiology [hp:0001311]
type: SIO_010056
comment: Phenotype [hp:0001311] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal nervous system electrophysiology
in dataset: phenotype

Peroneal muscle atrophy [hp:0009049]
type: SIO_010056
comment: Phenotype [hp:0009049] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peroneal muscle atrophy
in dataset: phenotype

Calcific mitral stenosis [hp:0200129]
type: SIO_010056
comment: Phenotype [hp:0200129] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcific mitral stenosis
in dataset: phenotype

Punctate keratitis [hp:0011859]
type: SIO_010056
comment: Phenotype [hp:0011859] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Punctate keratitis
in dataset: phenotype

Abnormal middle ear reflexes [hp:0004454]
type: SIO_010056
comment: Phenotype [hp:0004454] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal middle ear reflexes
in dataset: phenotype

Meckel diverticulum [hp:0002245]
type: SIO_010056
comment: Phenotype [hp:0002245] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Meckel diverticulum
in dataset: phenotype

Unexplained fevers [hp:0001955]
type: SIO_010056
comment: Phenotype [hp:0001955] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unexplained fevers
in dataset: phenotype

Increased variability in muscle fiber diameter [hp:0003557]
type: SIO_010056
comment: Phenotype [hp:0003557] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased variability in muscle fiber diameter
in dataset: phenotype

Hypersegmentation of neutrophil nuclei [hp:0004821]
type: SIO_010056
comment: Phenotype [hp:0004821] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypersegmentation of neutrophil nuclei
in dataset: phenotype

Metastatic angiosarcoma [hp:0200059]
type: SIO_010056
comment: Phenotype [hp:0200059] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metastatic angiosarcoma
in dataset: phenotype

Glutathione synthetase deficiency [hp:0003343]
type: SIO_010056
comment: Phenotype [hp:0003343] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glutathione synthetase deficiency
in dataset: phenotype

Hypergammaglobulinemia [hp:0010702]
type: SIO_010056
comment: Phenotype [hp:0010702] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypergammaglobulinemia
in dataset: phenotype

Cafe-au-lait spot [hp:0000957]
type: SIO_010056
comment: Phenotype [hp:0000957] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cafe-au-lait spot
in dataset: phenotype

Abnormal cortical bone morphology [hp:0003103]
type: SIO_010056
comment: Phenotype [hp:0003103] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal cortical bone morphology
in dataset: phenotype

Periodic paralysis [hp:0003768]
type: SIO_010056
comment: Phenotype [hp:0003768] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Periodic paralysis
in dataset: phenotype

Neutrophil inclusion bodies [hp:0008264]
type: SIO_010056
comment: Phenotype [hp:0008264] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neutrophil inclusion bodies
in dataset: phenotype

Episodic fever [hp:0001954]
type: SIO_010056
comment: Phenotype [hp:0001954] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic fever
in dataset: phenotype

Flat acetabular roof [hp:0003180]
type: SIO_010056
comment: Phenotype [hp:0003180] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flat acetabular roof
in dataset: phenotype

Spastic diplegia [hp:0001264]
type: SIO_010056
comment: Phenotype [hp:0001264] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spastic diplegia
in dataset: phenotype

Short phalanx of finger [hp:0009803]
type: SIO_010056
comment: Phenotype [hp:0009803] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short phalanx of finger
in dataset: phenotype

Exotropia [hp:0000577]
type: SIO_010056
comment: Phenotype [hp:0000577] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exotropia
in dataset: phenotype

Dysmetria [hp:0001310]
type: SIO_010056
comment: Phenotype [hp:0001310] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysmetria
in dataset: phenotype

Glomerulopathy [hp:0100820]
type: SIO_010056
comment: Phenotype [hp:0100820] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glomerulopathy
in dataset: phenotype

Pericardial effusion [hp:0001698]
type: SIO_010056
comment: Phenotype [hp:0001698] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pericardial effusion
in dataset: phenotype

Biventricular hypertrophy [hp:0200128]
type: SIO_010056
comment: Phenotype [hp:0200128] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Biventricular hypertrophy
in dataset: phenotype

Overfolding of the superior helices [hp:0004453]
type: SIO_010056
comment: Phenotype [hp:0004453] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Overfolding of the superior helices
in dataset: phenotype

Abnormality of the duodenum [hp:0002246]
type: SIO_010056
comment: Phenotype [hp:0002246] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the duodenum
in dataset: phenotype

Midline facial cleft [hp:0100629]
type: SIO_010056
comment: Phenotype [hp:0100629] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Midline facial cleft
in dataset: phenotype

Reduced factor IX activity [hp:0011858]
type: SIO_010056
comment: Phenotype [hp:0011858] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced factor IX activity
in dataset: phenotype

Thyroid defect in oxidation and organification of iodide [hp:0008263]
type: SIO_010056
comment: Phenotype [hp:0008263] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thyroid defect in oxidation and organification of iodide
in dataset: phenotype

Stillbirth [hp:0003826]
type: SIO_010056
comment: Phenotype [hp:0003826] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stillbirth
in dataset: phenotype

Acanthosis nigricans [hp:0000956]
type: SIO_010056
comment: Phenotype [hp:0000956] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acanthosis nigricans
in dataset: phenotype

Increased carrying angle [hp:0003102]
type: SIO_010056
comment: Phenotype [hp:0003102] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased carrying angle
in dataset: phenotype

Abnormal immunoglobulin level [hp:0010701]
type: SIO_010056
comment: Phenotype [hp:0010701] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal immunoglobulin level
in dataset: phenotype

Sensorimotor neuropathy [hp:0007141]
type: SIO_010056
comment: Phenotype [hp:0007141] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sensorimotor neuropathy
in dataset: phenotype

Corpus cavernosum sclerosis [hp:0100624]
type: SIO_010056
comment: Phenotype [hp:0100624] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corpus cavernosum sclerosis
in dataset: phenotype

Thick eyebrow [hp:0000574]
type: SIO_010056
comment: Phenotype [hp:0000574] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thick eyebrow
in dataset: phenotype

Vertebral hypoplasia [hp:0008417]
type: SIO_010056
comment: Phenotype [hp:0008417] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vertebral hypoplasia
in dataset: phenotype

Aplasia of the phalanges of the hand [hp:0009802]
type: SIO_010056
comment: Phenotype [hp:0009802] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the phalanges of the hand
in dataset: phenotype

Large foramen magnum [hp:0002700]
type: SIO_010056
comment: Phenotype [hp:0002700] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large foramen magnum
in dataset: phenotype

Hyperinsulinemia [hp:0000842]
type: SIO_010056
comment: Phenotype [hp:0000842] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperinsulinemia
in dataset: phenotype

Multiple rows of eyelashes [hp:0008496]
type: SIO_010056
comment: Phenotype [hp:0008496] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple rows of eyelashes
in dataset: phenotype

Myokymia [hp:0002411]
type: SIO_010056
comment: Phenotype [hp:0002411] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myokymia
in dataset: phenotype

Hypotriglyceridemia [hp:0012153]
type: SIO_010056
comment: Phenotype [hp:0012153] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypotriglyceridemia
in dataset: phenotype

Fragmented, irregular epiphyses [hp:0005063]
type: SIO_010056
comment: Phenotype [hp:0005063] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fragmented, irregular epiphyses
in dataset: phenotype

Posterior scalloping of vertebral bodies [hp:0005121]
type: SIO_010056
comment: Phenotype [hp:0005121] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior scalloping of vertebral bodies
in dataset: phenotype

Multiple prenatal fractures [hp:0005855]
type: SIO_010056
comment: Phenotype [hp:0005855] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple prenatal fractures
in dataset: phenotype

Trapezoidal distal femoral condyles [hp:0006432]
type: SIO_010056
comment: Phenotype [hp:0006432] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Trapezoidal distal femoral condyles
in dataset: phenotype

Absent vas deferens [hp:0012873]
type: SIO_010056
comment: Phenotype [hp:0012873] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent vas deferens
in dataset: phenotype

Junctional split [hp:0003341]
type: SIO_010056
comment: Phenotype [hp:0003341] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Junctional split
in dataset: phenotype

Juvenile epithelial corneal dystrophy [hp:0007755]
type: SIO_010056
comment: Phenotype [hp:0007755] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Juvenile epithelial corneal dystrophy
in dataset: phenotype

1-5 finger syndactyly [hp:0010708]
type: SIO_010056
comment: Phenotype [hp:0010708] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 1-5 finger syndactyly
in dataset: phenotype

Abnormality of the cerebellum [hp:0001317]
type: SIO_010056
comment: Phenotype [hp:0001317] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the cerebellum
in dataset: phenotype

Anisopoikilocytosis [hp:0004823]
type: SIO_010056
comment: Phenotype [hp:0004823] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anisopoikilocytosis
in dataset: phenotype

Muscle fiber splitting [hp:0003555]
type: SIO_010056
comment: Phenotype [hp:0003555] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscle fiber splitting
in dataset: phenotype

Thyroid-stimulating hormone excess [hp:0002925]
type: SIO_010056
comment: Phenotype [hp:0002925] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thyroid-stimulating hormone excess
in dataset: phenotype

Scotoma [hp:0000575]
type: SIO_010056
comment: Phenotype [hp:0000575] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scotoma
in dataset: phenotype

Symmetric lesions of the basal ganglia [hp:0007039]
type: SIO_010056
comment: Phenotype [hp:0007039] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Symmetric lesions of the basal ganglia
in dataset: phenotype

Hyperactive renin-angiotensin system [hp:0000841]
type: SIO_010056
comment: Phenotype [hp:0000841] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperactive renin-angiotensin system
in dataset: phenotype

Delayed eruption of primary teeth [hp:0000680]
type: SIO_010056
comment: Phenotype [hp:0000680] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed eruption of primary teeth
in dataset: phenotype

Reduced thyroxin-binding globulin [hp:0012509]
type: SIO_010056
comment: Phenotype [hp:0012509] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced thyroxin-binding globulin
in dataset: phenotype

Inferior lens subluxation [hp:0008494]
type: SIO_010056
comment: Phenotype [hp:0008494] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inferior lens subluxation
in dataset: phenotype

Edema of the dorsum of feet [hp:0012098]
type: SIO_010056
comment: Phenotype [hp:0012098] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Edema of the dorsum of feet
in dataset: phenotype

Single transverse palmar crease [hp:0000954]
type: SIO_010056
comment: Phenotype [hp:0000954] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Single transverse palmar crease
in dataset: phenotype

Proximal femoral metaphyseal abnormality [hp:0006431]
type: SIO_010056
comment: Phenotype [hp:0006431] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal femoral metaphyseal abnormality
in dataset: phenotype

Variable expressivity [hp:0003828]
type: SIO_010056
comment: Phenotype [hp:0003828] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Variable expressivity
in dataset: phenotype

Macular dystrophy [hp:0007754]
type: SIO_010056
comment: Phenotype [hp:0007754] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macular dystrophy
in dataset: phenotype

Midline nasal groove [hp:0004112]
type: SIO_010056
comment: Phenotype [hp:0004112] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Midline nasal groove
in dataset: phenotype

Flat face [hp:0012368]
type: SIO_010056
comment: Phenotype [hp:0012368] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flat face
in dataset: phenotype

Decreased circulating aldosterone level [hp:0002924]
type: SIO_010056
comment: Phenotype [hp:0002924] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased circulating aldosterone level
in dataset: phenotype

Type 2 muscle fiber atrophy [hp:0003554]
type: SIO_010056
comment: Phenotype [hp:0003554] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type 2 muscle fiber atrophy
in dataset: phenotype

Congenital macroorchidism [hp:0008640]
type: SIO_010056
comment: Phenotype [hp:0008640] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital macroorchidism
in dataset: phenotype

Reduced tendon reflexes [hp:0001315]
type: SIO_010056
comment: Phenotype [hp:0001315] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced tendon reflexes
in dataset: phenotype

Abnormality of the pharynx [hp:0000600]
type: SIO_010056
comment: Phenotype [hp:0000600] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the pharynx
in dataset: phenotype

Episodic ammonia intoxication [hp:0001951]
type: SIO_010056
comment: Phenotype [hp:0001951] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic ammonia intoxication
in dataset: phenotype

Steatorrhea [hp:0002570]
type: SIO_010056
comment: Phenotype [hp:0002570] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Steatorrhea
in dataset: phenotype

Neoplasm of the thyroid gland [hp:0100031]
type: SIO_010056
comment: Phenotype [hp:0100031] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the thyroid gland
in dataset: phenotype

Exercise-induced myoglobinuria [hp:0008305]
type: SIO_010056
comment: Phenotype [hp:0008305] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exercise-induced myoglobinuria
in dataset: phenotype

Neoplasm of the rectum [hp:0100743]
type: SIO_010056
comment: Phenotype [hp:0100743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the rectum
in dataset: phenotype

Visual loss [hp:0000572]
type: SIO_010056
comment: Phenotype [hp:0000572] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Visual loss
in dataset: phenotype

Substantia nigra gliosis [hp:0011960]
type: SIO_010056
comment: Phenotype [hp:0011960] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Substantia nigra gliosis
in dataset: phenotype

Metamorphopsia [hp:0012508]
type: SIO_010056
comment: Phenotype [hp:0012508] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metamorphopsia
in dataset: phenotype

Adrenogenital syndrome [hp:0000840]
type: SIO_010056
comment: Phenotype [hp:0000840] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenogenital syndrome
in dataset: phenotype

Hyperpigmentation of the skin [hp:0000953]
type: SIO_010056
comment: Phenotype [hp:0000953] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperpigmentation of the skin
in dataset: phenotype

Maternal diabetes [hp:0009800]
type: SIO_010056
comment: Phenotype [hp:0009800] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Maternal diabetes
in dataset: phenotype

Anterior clefting of vertebral bodies [hp:0009761]
type: SIO_010056
comment: Phenotype [hp:0009761] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior clefting of vertebral bodies
in dataset: phenotype

Varicocele [hp:0012871]
type: SIO_010056
comment: Phenotype [hp:0012871] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Varicocele
in dataset: phenotype

Hypoplasia of proximal radius [hp:0006434]
type: SIO_010056
comment: Phenotype [hp:0006434] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of proximal radius
in dataset: phenotype

Hemothorax [hp:0012151]
type: SIO_010056
comment: Phenotype [hp:0012151] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemothorax
in dataset: phenotype

Incomplete penetrance [hp:0003829]
type: SIO_010056
comment: Phenotype [hp:0003829] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Incomplete penetrance
in dataset: phenotype

Anterior concavity of thoracic vertebrae [hp:0004611]
type: SIO_010056
comment: Phenotype [hp:0004611] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior concavity of thoracic vertebrae
in dataset: phenotype

Dilatated internal auditory canal [hp:0004458]
type: SIO_010056
comment: Phenotype [hp:0004458] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dilatated internal auditory canal
in dataset: phenotype

Cellulitis due to immunodeficiency [hp:0003553]
type: SIO_010056
comment: Phenotype [hp:0003553] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cellulitis due to immunodeficiency
in dataset: phenotype

Chronic hepatic failure [hp:0100626]
type: SIO_010056
comment: Phenotype [hp:0100626] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic hepatic failure
in dataset: phenotype

Hypoplastic nasal tip [hp:0005278]
type: SIO_010056
comment: Phenotype [hp:0005278] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic nasal tip
in dataset: phenotype

Genital hernia [hp:0100823]
type: SIO_010056
comment: Phenotype [hp:0100823] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Genital hernia
in dataset: phenotype

Histidinuria [hp:0002927]
type: SIO_010056
comment: Phenotype [hp:0002927] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Histidinuria
in dataset: phenotype

Hypoplasia of choroid [hp:0007757]
type: SIO_010056
comment: Phenotype [hp:0007757] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of choroid
in dataset: phenotype

Melena [hp:0002249]
type: SIO_010056
comment: Phenotype [hp:0002249] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Melena
in dataset: phenotype

Pharyngeal edema [hp:0011855]
type: SIO_010056
comment: Phenotype [hp:0011855] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pharyngeal edema
in dataset: phenotype

Achalasia [hp:0002571]
type: SIO_010056
comment: Phenotype [hp:0002571] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Achalasia
in dataset: phenotype

Six lumbar vertebrae [hp:0008416]
type: SIO_010056
comment: Phenotype [hp:0008416] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Six lumbar vertebrae
in dataset: phenotype

Mesoaxial foot polydactyly [hp:0010112]
type: SIO_010056
comment: Phenotype [hp:0010112] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mesoaxial foot polydactyly
in dataset: phenotype

Absence of acoustic reflex [hp:0008529]
type: SIO_010056
comment: Phenotype [hp:0008529] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of acoustic reflex
in dataset: phenotype

Respiratory alkalosis [hp:0001950]
type: SIO_010056
comment: Phenotype [hp:0001950] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Respiratory alkalosis
in dataset: phenotype

Dysarthria [hp:0001260]
type: SIO_010056
comment: Phenotype [hp:0001260] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysarthria
in dataset: phenotype

Retinal hemorrhage [hp:0000573]
type: SIO_010056
comment: Phenotype [hp:0000573] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal hemorrhage
in dataset: phenotype

Vascular neoplasm [hp:0100742]
type: SIO_010056
comment: Phenotype [hp:0100742] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vascular neoplasm
in dataset: phenotype

Folate-unresponsive megaloblastic anemia [hp:0004826]
type: SIO_010056
comment: Phenotype [hp:0004826] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Folate-unresponsive megaloblastic anemia
in dataset: phenotype

Jaundice [hp:0000952]
type: SIO_010056
comment: Phenotype [hp:0000952] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Jaundice
in dataset: phenotype

Antecubital pterygium [hp:0009760]
type: SIO_010056
comment: Phenotype [hp:0009760] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Antecubital pterygium
in dataset: phenotype

Camptodactyly of finger [hp:0100490]
type: SIO_010056
comment: Phenotype [hp:0100490] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Camptodactyly of finger
in dataset: phenotype

Spina bifida [hp:0002414]
type: SIO_010056
comment: Phenotype [hp:0002414] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spina bifida
in dataset: phenotype

4-5 finger syndactyly [hp:0010705]
type: SIO_010056
comment: Phenotype [hp:0010705] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 4-5 finger syndactyly
in dataset: phenotype

Muscle stiffness [hp:0003552]
type: SIO_010056
comment: Phenotype [hp:0003552] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscle stiffness
in dataset: phenotype

Foveoschisis [hp:0012152]
type: SIO_010056
comment: Phenotype [hp:0012152] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Foveoschisis
in dataset: phenotype

Enlarged thorax [hp:0100625]
type: SIO_010056
comment: Phenotype [hp:0100625] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged thorax
in dataset: phenotype

Shortening of the tibia [hp:0006436]
type: SIO_010056
comment: Phenotype [hp:0006436] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shortening of the tibia
in dataset: phenotype

Ophthalmoplegia [hp:0000602]
type: SIO_010056
comment: Phenotype [hp:0000602] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ophthalmoplegia
in dataset: phenotype

Onychomycosis [hp:0012203]
type: SIO_010056
comment: Phenotype [hp:0012203] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Onychomycosis
in dataset: phenotype

Elevated plasma citrulline [hp:0011966]
type: SIO_010056
comment: Phenotype [hp:0011966] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated plasma citrulline
in dataset: phenotype

Flaring of lower rib cage [hp:0006589]
type: SIO_010056
comment: Phenotype [hp:0006589] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flaring of lower rib cage
in dataset: phenotype

Genu valgum [hp:0002857]
type: SIO_010056
comment: Phenotype [hp:0002857] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Genu valgum
in dataset: phenotype

Underdeveloped tragus [hp:0011272]
type: SIO_010056
comment: Phenotype [hp:0011272] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Underdeveloped tragus
in dataset: phenotype

Cheilitis [hp:0100825]
type: SIO_010056
comment: Phenotype [hp:0100825] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cheilitis
in dataset: phenotype

Increased hemoglobin [hp:0001900]
type: SIO_010056
comment: Phenotype [hp:0001900] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased hemoglobin
in dataset: phenotype

Follicular thyroid carcinoma [hp:0006731]
type: SIO_010056
comment: Phenotype [hp:0006731] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Follicular thyroid carcinoma
in dataset: phenotype

Decreased serum complement factor B [hp:0005416]
type: SIO_010056
comment: Phenotype [hp:0005416] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased serum complement factor B
in dataset: phenotype

Severe platyspondyly [hp:0004565]
type: SIO_010056
comment: Phenotype [hp:0004565] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe platyspondyly
in dataset: phenotype

Adrenal insufficiency [hp:0000846]
type: SIO_010056
comment: Phenotype [hp:0000846] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenal insufficiency
in dataset: phenotype

Multiple joint dislocation [hp:0012095]
type: SIO_010056
comment: Phenotype [hp:0012095] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple joint dislocation
in dataset: phenotype

Perioral eczema [hp:0011127]
type: SIO_010056
comment: Phenotype [hp:0011127] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Perioral eczema
in dataset: phenotype

Axonal regeneration [hp:0003450]
type: SIO_010056
comment: Phenotype [hp:0003450] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Axonal regeneration
in dataset: phenotype

Hemihypotrophy of lower limb [hp:0200053]
type: SIO_010056
comment: Phenotype [hp:0200053] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemihypotrophy of lower limb
in dataset: phenotype

Muscular subvalvular aortic stenosis [hp:0001691]
type: SIO_010056
comment: Phenotype [hp:0001691] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscular subvalvular aortic stenosis
in dataset: phenotype

Small pituitary gland [hp:0012506]
type: SIO_010056
comment: Phenotype [hp:0012506] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small pituitary gland
in dataset: phenotype

Distal upper limb amyotrophy [hp:0007149]
type: SIO_010056
comment: Phenotype [hp:0007149] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal upper limb amyotrophy
in dataset: phenotype

Short distal phalanx of the thumb [hp:0009650]
type: SIO_010056
comment: Phenotype [hp:0009650] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short distal phalanx of the thumb
in dataset: phenotype

Abnormality of saccadic eye movements [hp:0000570]
type: SIO_010056
comment: Phenotype [hp:0000570] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of saccadic eye movements
in dataset: phenotype

Increased red cell hemolysis by shear stress [hp:0008269]
type: SIO_010056
comment: Phenotype [hp:0008269] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased red cell hemolysis by shear stress
in dataset: phenotype

Intermittent jaundice [hp:0001046]
type: SIO_010056
comment: Phenotype [hp:0001046] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intermittent jaundice
in dataset: phenotype

Abnormality of the skin [hp:0000951]
type: SIO_010056
comment: Phenotype [hp:0000951] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the skin
in dataset: phenotype

Grayish enamel [hp:0000683]
type: SIO_010056
comment: Phenotype [hp:0000683] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Grayish enamel
in dataset: phenotype

Absent nares [hp:0100596]
type: SIO_010056
comment: Phenotype [hp:0100596] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent nares
in dataset: phenotype

Oral ulcer [hp:0000155]
type: SIO_010056
comment: Phenotype [hp:0000155] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oral ulcer
in dataset: phenotype

Tracheal stenosis [hp:0002777]
type: SIO_010056
comment: Phenotype [hp:0002777] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tracheal stenosis
in dataset: phenotype

Abnormality of the temporal bone [hp:0009911]
type: SIO_010056
comment: Phenotype [hp:0009911] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the temporal bone
in dataset: phenotype

Meningioma [hp:0002858]
type: SIO_010056
comment: Phenotype [hp:0002858] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Meningioma
in dataset: phenotype

Deja vu [hp:0012005]
type: SIO_010056
comment: Phenotype [hp:0012005] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deja vu
in dataset: phenotype

Gaze-evoked horizontal nystagmus [hp:0007979]
type: SIO_010056
comment: Phenotype [hp:0007979] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gaze-evoked horizontal nystagmus
in dataset: phenotype

Increased serum bile acid concentration [hp:0012202]
type: SIO_010056
comment: Phenotype [hp:0012202] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased serum bile acid concentration
in dataset: phenotype

Anisocytosis [hp:0011273]
type: SIO_010056
comment: Phenotype [hp:0011273] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anisocytosis
in dataset: phenotype

Polycythemia [hp:0001901]
type: SIO_010056
comment: Phenotype [hp:0001901] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polycythemia
in dataset: phenotype

Lipogranulomatosis [hp:0040139]
type: SIO_010056
comment: Phenotype [hp:0040139] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lipogranulomatosis
in dataset: phenotype

Hypoplasia of the fovea [hp:0007750]
type: SIO_010056
comment: Phenotype [hp:0007750] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the fovea
in dataset: phenotype

Abnormal vestibulo-ocular reflex [hp:0007670]
type: SIO_010056
comment: Phenotype [hp:0007670] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal vestibulo-ocular reflex
in dataset: phenotype

Growth hormone excess [hp:0000845]
type: SIO_010056
comment: Phenotype [hp:0000845] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Growth hormone excess
in dataset: phenotype

Decreased number of CD8+ T cells [hp:0005415]
type: SIO_010056
comment: Phenotype [hp:0005415] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased number of CD8+ T cells
in dataset: phenotype

Spina bifida occulta at S1 [hp:0004614]
type: SIO_010056
comment: Phenotype [hp:0004614] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spina bifida occulta at S1
in dataset: phenotype

High-grade hypermetropia [hp:0008499]
type: SIO_010056
comment: Phenotype [hp:0008499] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High-grade hypermetropia
in dataset: phenotype

Primary atrial arrhythmia [hp:0001692]
type: SIO_010056
comment: Phenotype [hp:0001692] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Primary atrial arrhythmia
in dataset: phenotype

Vitiligo [hp:0001045]
type: SIO_010056
comment: Phenotype [hp:0001045] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vitiligo
in dataset: phenotype

Hypometric saccades [hp:0000571]
type: SIO_010056
comment: Phenotype [hp:0000571] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypometric saccades
in dataset: phenotype

Decreased circulating ACTH level [hp:0002920]
type: SIO_010056
comment: Phenotype [hp:0002920] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased circulating ACTH level
in dataset: phenotype

Prominent calcaneus [hp:0012428]
type: SIO_010056
comment: Phenotype [hp:0012428] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent calcaneus
in dataset: phenotype

Delayed eruption of teeth [hp:0000684]
type: SIO_010056
comment: Phenotype [hp:0000684] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed eruption of teeth
in dataset: phenotype

Abnormality of the rib cage [hp:0001547]
type: SIO_010056
comment: Phenotype [hp:0001547] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the rib cage
in dataset: phenotype

Congenital sensorineural hearing impairment [hp:0008527]
type: SIO_010056
comment: Phenotype [hp:0008527] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital sensorineural hearing impairment
in dataset: phenotype

Hypotelorism [hp:0000601]
type: SIO_010056
comment: Phenotype [hp:0000601] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypotelorism
in dataset: phenotype

Wide mouth [hp:0000154]
type: SIO_010056
comment: Phenotype [hp:0000154] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Wide mouth
in dataset: phenotype

Denervation of the diaphragm [hp:0009109]
type: SIO_010056
comment: Phenotype [hp:0009109] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Denervation of the diaphragm
in dataset: phenotype

Joint hyperflexibility [hp:0005692]
type: SIO_010056
comment: Phenotype [hp:0005692] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Joint hyperflexibility
in dataset: phenotype

Cerulean cataract [hp:0007976]
type: SIO_010056
comment: Phenotype [hp:0007976] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerulean cataract
in dataset: phenotype

Giant platelets [hp:0001902]
type: SIO_010056
comment: Phenotype [hp:0001902] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Giant platelets
in dataset: phenotype

Rheumatoid factor positive [hp:0002923]
type: SIO_010056
comment: Phenotype [hp:0002923] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rheumatoid factor positive
in dataset: phenotype

Recurrent mycobacterial infections [hp:0011274]
type: SIO_010056
comment: Phenotype [hp:0011274] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent mycobacterial infections
in dataset: phenotype

Reduced prothrombin activity [hp:0012201]
type: SIO_010056
comment: Phenotype [hp:0012201] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced prothrombin activity
in dataset: phenotype

Lymphocytosis [hp:0100827]
type: SIO_010056
comment: Phenotype [hp:0100827] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lymphocytosis
in dataset: phenotype

Enlargement of the distal femoral epiphysis [hp:0006438]
type: SIO_010056
comment: Phenotype [hp:0006438] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlargement of the distal femoral epiphysis
in dataset: phenotype

Acute megakaryocytic leukemia [hp:0006733]
type: SIO_010056
comment: Phenotype [hp:0006733] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute megakaryocytic leukemia
in dataset: phenotype

Hyperapobetalipoproteinemia [hp:0008158]
type: SIO_010056
comment: Phenotype [hp:0008158] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperapobetalipoproteinemia
in dataset: phenotype

Limited elbow flexion/extension [hp:0005060]
type: SIO_010056
comment: Phenotype [hp:0005060] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited elbow flexion/extension
in dataset: phenotype

Abnormality of the mouth [hp:0000153]
type: SIO_010056
comment: Phenotype [hp:0000153] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the mouth
in dataset: phenotype

Tricuspid stenosis [hp:0010446]
type: SIO_010056
comment: Phenotype [hp:0010446] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tricuspid stenosis
in dataset: phenotype

Prominent umbilicus [hp:0001544]
type: SIO_010056
comment: Phenotype [hp:0001544] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent umbilicus
in dataset: phenotype

Weak cry [hp:0001612]
type: SIO_010056
comment: Phenotype [hp:0001612] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Weak cry
in dataset: phenotype

Intervertebral disc degeneration [hp:0008419]
type: SIO_010056
comment: Phenotype [hp:0008419] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intervertebral disc degeneration
in dataset: phenotype

Calcinosis [hp:0003761]
type: SIO_010056
comment: Phenotype [hp:0003761] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcinosis
in dataset: phenotype

Comodogenic acne [hp:0040137]
type: SIO_010056
comment: Phenotype [hp:0040137] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Comodogenic acne
in dataset: phenotype

Optic disc drusen [hp:0012426]
type: SIO_010056
comment: Phenotype [hp:0012426] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Optic disc drusen
in dataset: phenotype

Valgus hand deformity [hp:0006228]
type: SIO_010056
comment: Phenotype [hp:0006228] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Valgus hand deformity
in dataset: phenotype

Anemia [hp:0001903]
type: SIO_010056
comment: Phenotype [hp:0001903] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anemia
in dataset: phenotype

2-4 finger syndactyly [hp:0010709]
type: SIO_010056
comment: Phenotype [hp:0010709] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 2-4 finger syndactyly
in dataset: phenotype

Disproportionate prominence of the femoral medial condyle [hp:0006437]
type: SIO_010056
comment: Phenotype [hp:0006437] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Disproportionate prominence of the femoral medial condyle
in dataset: phenotype

Anal fistula [hp:0010447]
type: SIO_010056
comment: Phenotype [hp:0010447] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anal fistula
in dataset: phenotype

Central scotoma [hp:0000603]
type: SIO_010056
comment: Phenotype [hp:0000603] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Central scotoma
in dataset: phenotype

Cleft vertebral arch [hp:0004616]
type: SIO_010056
comment: Phenotype [hp:0004616] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cleft vertebral arch
in dataset: phenotype

Weakness of facial musculature [hp:0030319]
type: SIO_010056
comment: Phenotype [hp:0030319] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Weakness of facial musculature
in dataset: phenotype

Recurrent mycobacterium avium complex infections [hp:0011275]
type: SIO_010056
comment: Phenotype [hp:0011275] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent mycobacterium avium complex infections
in dataset: phenotype

Pear-shaped vertebrae [hp:0004566]
type: SIO_010056
comment: Phenotype [hp:0004566] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pear-shaped vertebrae
in dataset: phenotype

Hyperparathyroidism [hp:0000843]
type: SIO_010056
comment: Phenotype [hp:0000843] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperparathyroidism
in dataset: phenotype

Aqueductal stenosis [hp:0002410]
type: SIO_010056
comment: Phenotype [hp:0002410] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aqueductal stenosis
in dataset: phenotype

Triangular epiphysis of the proximal phalanx of the 2nd finger [hp:0009534]
type: SIO_010056
comment: Phenotype [hp:0009534] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular epiphysis of the proximal phalanx of the 2nd finger
in dataset: phenotype

Percussion-induced rapid rolling muscle contractions (PIRC) [hp:0003760]
type: SIO_010056
comment: Phenotype [hp:0003760] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Percussion-induced rapid rolling muscle contractions (PIRC)
in dataset: phenotype

Anteriorly placed anus [hp:0001545]
type: SIO_010056
comment: Phenotype [hp:0001545] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anteriorly placed anus
in dataset: phenotype

Prominent scalp veins [hp:0001043]
type: SIO_010056
comment: Phenotype [hp:0001043] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent scalp veins
in dataset: phenotype

Nasal speech [hp:0001611]
type: SIO_010056
comment: Phenotype [hp:0001611] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nasal speech
in dataset: phenotype

Increased CSF protein [hp:0002922]
type: SIO_010056
comment: Phenotype [hp:0002922] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased CSF protein
in dataset: phenotype

Axial malrotation of the kidney [hp:0004717]
type: SIO_010056
comment: Phenotype [hp:0004717] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Axial malrotation of the kidney
in dataset: phenotype

Abnormality of dental enamel [hp:0000682]
type: SIO_010056
comment: Phenotype [hp:0000682] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of dental enamel
in dataset: phenotype

Prolonged prothrombin time [hp:0008151]
type: SIO_010056
comment: Phenotype [hp:0008151] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolonged prothrombin time
in dataset: phenotype

Congenital pseudoarthrosis of the clavicle [hp:0006585]
type: SIO_010056
comment: Phenotype [hp:0006585] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital pseudoarthrosis of the clavicle
in dataset: phenotype

Congenital hypertrophy of left ventricle [hp:0005129]
type: SIO_010056
comment: Phenotype [hp:0005129] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital hypertrophy of left ventricle
in dataset: phenotype

Anuria [hp:0100519]
type: SIO_010056
comment: Phenotype [hp:0100519] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anuria
in dataset: phenotype

Hypoalbuminemia [hp:0003073]
type: SIO_010056
comment: Phenotype [hp:0003073] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoalbuminemia
in dataset: phenotype

Marcus Gunn pupil [hp:0200057]
type: SIO_010056
comment: Phenotype [hp:0200057] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Marcus Gunn pupil
in dataset: phenotype

Subarachnoid hemorrhage [hp:0002138]
type: SIO_010056
comment: Phenotype [hp:0002138] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subarachnoid hemorrhage
in dataset: phenotype

Partial fusion of proximal row of carpal bones [hp:0005694]
type: SIO_010056
comment: Phenotype [hp:0005694] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Partial fusion of proximal row of carpal bones
in dataset: phenotype

Platelet antibody positive [hp:0003454]
type: SIO_010056
comment: Phenotype [hp:0003454] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Platelet antibody positive
in dataset: phenotype

Galactorrhea [hp:0100829]
type: SIO_010056
comment: Phenotype [hp:0100829] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Galactorrhea
in dataset: phenotype

Prominent median palatal raphe [hp:0002708]
type: SIO_010056
comment: Phenotype [hp:0002708] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent median palatal raphe
in dataset: phenotype

High axial triradius [hp:0001042]
type: SIO_010056
comment: Phenotype [hp:0001042] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High axial triradius
in dataset: phenotype

EEG abnormality [hp:0002353]
type: SIO_010056
comment: Phenotype [hp:0002353] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EEG abnormality
in dataset: phenotype

Pulmonary insufficiency [hp:0010444]
type: SIO_010056
comment: Phenotype [hp:0010444] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary insufficiency
in dataset: phenotype

Reduced sperm motility [hp:0012207]
type: SIO_010056
comment: Phenotype [hp:0012207] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced sperm motility
in dataset: phenotype

Cardiac arrest [hp:0001695]
type: SIO_010056
comment: Phenotype [hp:0001695] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cardiac arrest
in dataset: phenotype

Widely spaced teeth [hp:0000687]
type: SIO_010056
comment: Phenotype [hp:0000687] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Widely spaced teeth
in dataset: phenotype

Venous thrombosis [hp:0004936]
type: SIO_010056
comment: Phenotype [hp:0004936] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Venous thrombosis
in dataset: phenotype

Widened metacarpal shaft [hp:0006012]
type: SIO_010056
comment: Phenotype [hp:0006012] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Widened metacarpal shaft
in dataset: phenotype

Aplasia/Hypoplasia of the pubic bone [hp:0009104]
type: SIO_010056
comment: Phenotype [hp:0009104] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the pubic bone
in dataset: phenotype

Butterfly vertebral arch [hp:0004617]
type: SIO_010056
comment: Phenotype [hp:0004617] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Butterfly vertebral arch
in dataset: phenotype

Bruxism [hp:0003763]
type: SIO_010056
comment: Phenotype [hp:0003763] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bruxism
in dataset: phenotype

Abducens palsy [hp:0011349]
type: SIO_010056
comment: Phenotype [hp:0011349] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abducens palsy
in dataset: phenotype

Dissecting aortic aneurysm [hp:0002622]
type: SIO_010056
comment: Phenotype [hp:0002622] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dissecting aortic aneurysm
in dataset: phenotype

Decreased T cell activation [hp:0005419]
type: SIO_010056
comment: Phenotype [hp:0005419] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased T cell activation
in dataset: phenotype

Small abnormally formed scapulae [hp:0006584]
type: SIO_010056
comment: Phenotype [hp:0006584] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small abnormally formed scapulae
in dataset: phenotype

Nonprogressive encephalopathy [hp:0007030]
type: SIO_010056
comment: Phenotype [hp:0007030] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonprogressive encephalopathy
in dataset: phenotype

Avascular necrosis of the capital femoral epiphysis [hp:0005743]
type: SIO_010056
comment: Phenotype [hp:0005743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Avascular necrosis of the capital femoral epiphysis
in dataset: phenotype

Antineutrophil antibody positivity [hp:0003453]
type: SIO_010056
comment: Phenotype [hp:0003453] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Antineutrophil antibody positivity
in dataset: phenotype

Truncal obesity [hp:0001956]
type: SIO_010056
comment: Phenotype [hp:0001956] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Truncal obesity
in dataset: phenotype

Supranuclear gaze palsy [hp:0000605]
type: SIO_010056
comment: Phenotype [hp:0000605] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Supranuclear gaze palsy
in dataset: phenotype

Arrhinencephaly [hp:0002139]
type: SIO_010056
comment: Phenotype [hp:0002139] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arrhinencephaly
in dataset: phenotype

Midline facial capillary hemangioma [hp:0007601]
type: SIO_010056
comment: Phenotype [hp:0007601] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Midline facial capillary hemangioma
in dataset: phenotype

Hyperglycemia [hp:0003074]
type: SIO_010056
comment: Phenotype [hp:0003074] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperglycemia
in dataset: phenotype

Elevated luteinizing hormone [hp:0011969]
type: SIO_010056
comment: Phenotype [hp:0011969] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated luteinizing hormone
in dataset: phenotype

EEG with generalized polyspikes [hp:0012001]
type: SIO_010056
comment: Phenotype [hp:0012001] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EEG with generalized polyspikes
in dataset: phenotype

Dysuria [hp:0100518]
type: SIO_010056
comment: Phenotype [hp:0100518] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysuria
in dataset: phenotype

Hypometric horizontal saccades [hp:0007975]
type: SIO_010056
comment: Phenotype [hp:0007975] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypometric horizontal saccades
in dataset: phenotype

Radioulnar dislocation [hp:0006439]
type: SIO_010056
comment: Phenotype [hp:0006439] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Radioulnar dislocation
in dataset: phenotype

Ulnar metaphyseal irregularity [hp:0004042]
type: SIO_010056
comment: Phenotype [hp:0004042] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ulnar metaphyseal irregularity
in dataset: phenotype

Aplasia of the middle phalanges of the toes [hp:0100387]
type: SIO_010056
comment: Phenotype [hp:0100387] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the middle phalanges of the toes
in dataset: phenotype

Facial erythema [hp:0001041]
type: SIO_010056
comment: Phenotype [hp:0001041] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial erythema
in dataset: phenotype

Hoarse voice (caused by tumor impingement) [hp:0001613]
type: SIO_010056
comment: Phenotype [hp:0001613] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hoarse voice (caused by tumor impingement)
in dataset: phenotype

Leukoencephalopathy [hp:0002352]
type: SIO_010056
comment: Phenotype [hp:0002352] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Leukoencephalopathy
in dataset: phenotype

Macroglossia [hp:0000158]
type: SIO_010056
comment: Phenotype [hp:0000158] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macroglossia
in dataset: phenotype

Cuboidal metacarpal [hp:0006011]
type: SIO_010056
comment: Phenotype [hp:0006011] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cuboidal metacarpal
in dataset: phenotype

Situs inversus totalis [hp:0001696]
type: SIO_010056
comment: Phenotype [hp:0001696] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Situs inversus totalis
in dataset: phenotype

Primum atrial septal defect [hp:0010445]
type: SIO_010056
comment: Phenotype [hp:0010445] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Primum atrial septal defect
in dataset: phenotype

Pulmonary artery aneurysm [hp:0004937]
type: SIO_010056
comment: Phenotype [hp:0004937] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary artery aneurysm
in dataset: phenotype

Gastroschisis [hp:0001543]
type: SIO_010056
comment: Phenotype [hp:0001543] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gastroschisis
in dataset: phenotype

Cyclopia [hp:0009914]
type: SIO_010056
comment: Phenotype [hp:0009914] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cyclopia
in dataset: phenotype

Atherosclerosis [hp:0002621]
type: SIO_010056
comment: Phenotype [hp:0002621] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atherosclerosis
in dataset: phenotype

Sandwich appearance of vertebral bodies [hp:0004618]
type: SIO_010056
comment: Phenotype [hp:0004618] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sandwich appearance of vertebral bodies
in dataset: phenotype

Uterus didelphys [hp:0003762]
type: SIO_010056
comment: Phenotype [hp:0003762] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Uterus didelphys
in dataset: phenotype

Small hand [hp:0200055]
type: SIO_010056
comment: Phenotype [hp:0200055] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small hand
in dataset: phenotype

Generalized osteoporosis with pathologic fractures [hp:0005744]
type: SIO_010056
comment: Phenotype [hp:0005744] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized osteoporosis with pathologic fractures
in dataset: phenotype

Straight clavicles [hp:0006587]
type: SIO_010056
comment: Phenotype [hp:0006587] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Straight clavicles
in dataset: phenotype

Increased circulating renin level [hp:0000848]
type: SIO_010056
comment: Phenotype [hp:0000848] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased circulating renin level
in dataset: phenotype

Increased serum iron [hp:0003452]
type: SIO_010056
comment: Phenotype [hp:0003452] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased serum iron
in dataset: phenotype

Periodic hypokalemic paresis [hp:0008153]
type: SIO_010056
comment: Phenotype [hp:0008153] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Periodic hypokalemic paresis
in dataset: phenotype

Broad-based gait [hp:0002136]
type: SIO_010056
comment: Phenotype [hp:0002136] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad-based gait
in dataset: phenotype

Renal malrotation [hp:0004712]
type: SIO_010056
comment: Phenotype [hp:0004712] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal malrotation
in dataset: phenotype

Increased spinal bone density [hp:0004563]
type: SIO_010056
comment: Phenotype [hp:0004563] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased spinal bone density
in dataset: phenotype

Polydipsia [hp:0001959]
type: SIO_010056
comment: Phenotype [hp:0001959] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polydipsia
in dataset: phenotype

Macular degeneration [hp:0000608]
type: SIO_010056
comment: Phenotype [hp:0000608] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macular degeneration
in dataset: phenotype

Rhabdomyosarcoma [hp:0002859]
type: SIO_010056
comment: Phenotype [hp:0002859] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rhabdomyosarcoma
in dataset: phenotype

Preauricular skin furrow [hp:0004450]
type: SIO_010056
comment: Phenotype [hp:0004450] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Preauricular skin furrow
in dataset: phenotype

Feeding difficulties [hp:0011968]
type: SIO_010056
comment: Phenotype [hp:0011968] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Feeding difficulties
in dataset: phenotype

Globozoospermia [hp:0012205]
type: SIO_010056
comment: Phenotype [hp:0012205] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Globozoospermia
in dataset: phenotype

Tortuous cerebral arteries [hp:0004938]
type: SIO_010056
comment: Phenotype [hp:0004938] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tortuous cerebral arteries
in dataset: phenotype

Multiple pterygia [hp:0001040]
type: SIO_010056
comment: Phenotype [hp:0001040] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple pterygia
in dataset: phenotype

Elbow ankylosis [hp:0003070]
type: SIO_010056
comment: Phenotype [hp:0003070] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elbow ankylosis
in dataset: phenotype

Tracheomalacia [hp:0002779]
type: SIO_010056
comment: Phenotype [hp:0002779] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tracheomalacia
in dataset: phenotype

Abnormality of the tongue [hp:0000157]
type: SIO_010056
comment: Phenotype [hp:0000157] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the tongue
in dataset: phenotype

Pulmonary edema [hp:0100598]
type: SIO_010056
comment: Phenotype [hp:0100598] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary edema
in dataset: phenotype

Diastasis recti [hp:0001540]
type: SIO_010056
comment: Phenotype [hp:0001540] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diastasis recti
in dataset: phenotype

Abnormally shaped carpal bones [hp:0006014]
type: SIO_010056
comment: Phenotype [hp:0006014] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormally shaped carpal bones
in dataset: phenotype

Polydactyly [hp:0010442]
type: SIO_010056
comment: Phenotype [hp:0010442] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polydactyly
in dataset: phenotype

Hypoplasia of teeth [hp:0000685]
type: SIO_010056
comment: Phenotype [hp:0000685] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of teeth
in dataset: phenotype

Psoriasis [hp:0003765]
type: SIO_010056
comment: Phenotype [hp:0003765] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Psoriasis
in dataset: phenotype

Abnormal pelvis bone ossification [hp:0009106]
type: SIO_010056
comment: Phenotype [hp:0009106] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal pelvis bone ossification
in dataset: phenotype

Cardiac shunt [hp:0001693]
type: SIO_010056
comment: Phenotype [hp:0001693] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cardiac shunt
in dataset: phenotype

Lumbar kyphoscoliosis [hp:0004619]
type: SIO_010056
comment: Phenotype [hp:0004619] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lumbar kyphoscoliosis
in dataset: phenotype

Increased rate of premature chromosome condensation [hp:0003451]
type: SIO_010056
comment: Phenotype [hp:0003451] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased rate of premature chromosome condensation
in dataset: phenotype

Abnormality of exocrine pancreas physiology [hp:0012092]
type: SIO_010056
comment: Phenotype [hp:0012092] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of exocrine pancreas physiology
in dataset: phenotype

Congenital foot contractures [hp:0005745]
type: SIO_010056
comment: Phenotype [hp:0005745] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital foot contractures
in dataset: phenotype

Macular scarring [hp:0200056]
type: SIO_010056
comment: Phenotype [hp:0200056] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macular scarring
in dataset: phenotype

Retinal dysplasia [hp:0007973]
type: SIO_010056
comment: Phenotype [hp:0007973] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal dysplasia
in dataset: phenotype

Tapering pointed ends of distal finger phalanges [hp:0006224]
type: SIO_010056
comment: Phenotype [hp:0006224] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tapering pointed ends of distal finger phalanges
in dataset: phenotype

Reversible renal failure [hp:0004713]
type: SIO_010056
comment: Phenotype [hp:0004713] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reversible renal failure
in dataset: phenotype

Beaking of vertebral bodies T12-L3 [hp:0004562]
type: SIO_010056
comment: Phenotype [hp:0004562] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Beaking of vertebral bodies T12-L3
in dataset: phenotype

Hoarse cry [hp:0001615]
type: SIO_010056
comment: Phenotype [hp:0001615] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hoarse cry
in dataset: phenotype

Periorbital wrinkles [hp:0000607]
type: SIO_010056
comment: Phenotype [hp:0000607] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Periorbital wrinkles
in dataset: phenotype

Palate telangiectasia [hp:0002707]
type: SIO_010056
comment: Phenotype [hp:0002707] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palate telangiectasia
in dataset: phenotype

Freckles in sun-exposed areas [hp:0007603]
type: SIO_010056
comment: Phenotype [hp:0007603] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Freckles in sun-exposed areas
in dataset: phenotype

Hypercalcemia [hp:0003072]
type: SIO_010056
comment: Phenotype [hp:0003072] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypercalcemia
in dataset: phenotype

Nonketotic hypoglycemia [hp:0001958]
type: SIO_010056
comment: Phenotype [hp:0001958] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonketotic hypoglycemia
in dataset: phenotype

Recurrent vulvovaginal candidiasis [hp:0012204]
type: SIO_010056
comment: Phenotype [hp:0012204] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent vulvovaginal candidiasis
in dataset: phenotype

Ascites [hp:0001541]
type: SIO_010056
comment: Phenotype [hp:0001541] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ascites
in dataset: phenotype

Abnormality of the tragus [hp:0009912]
type: SIO_010056
comment: Phenotype [hp:0009912] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the tragus
in dataset: phenotype

Right-to-left shunt [hp:0001694]
type: SIO_010056
comment: Phenotype [hp:0001694] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Right-to-left shunt
in dataset: phenotype

Bifid femur [hp:0010443]
type: SIO_010056
comment: Phenotype [hp:0010443] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid femur
in dataset: phenotype

Flattened epiphysis [hp:0003071]
type: SIO_010056
comment: Phenotype [hp:0003071] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flattened epiphysis
in dataset: phenotype

Cerebellar cyst [hp:0002350]
type: SIO_010056
comment: Phenotype [hp:0002350] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebellar cyst
in dataset: phenotype

Cerebellar dysplasia [hp:0007033]
type: SIO_010056
comment: Phenotype [hp:0007033] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebellar dysplasia
in dataset: phenotype

Nevus [hp:0003764]
type: SIO_010056
comment: Phenotype [hp:0003764] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nevus
in dataset: phenotype

Overriding aorta [hp:0002623]
type: SIO_010056
comment: Phenotype [hp:0002623] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Overriding aorta
in dataset: phenotype

Abnormal ossification involving the femoral head and neck [hp:0009107]
type: SIO_010056
comment: Phenotype [hp:0009107] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal ossification involving the femoral head and neck
in dataset: phenotype

Mucopolysacchariduria [hp:0008155]
type: SIO_010056
comment: Phenotype [hp:0008155] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mucopolysacchariduria
in dataset: phenotype

Progressive neurologic deterioration [hp:0002344]
type: SIO_010056
comment: Phenotype [hp:0002344] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive neurologic deterioration
in dataset: phenotype

Deep venous thrombosis [hp:0002625]
type: SIO_010056
comment: Phenotype [hp:0002625] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deep venous thrombosis
in dataset: phenotype

Limitation of knee mobility [hp:0010501]
type: SIO_010056
comment: Phenotype [hp:0010501] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limitation of knee mobility
in dataset: phenotype

Laryngeal calcification [hp:0008754]
type: SIO_010056
comment: Phenotype [hp:0008754] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laryngeal calcification
in dataset: phenotype

Progressive hypotrichosis [hp:0002296]
type: SIO_010056
comment: Phenotype [hp:0002296] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive hypotrichosis
in dataset: phenotype

Aplasia/Hypoplasia of the earlobes [hp:0009906]
type: SIO_010056
comment: Phenotype [hp:0009906] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the earlobes
in dataset: phenotype

Depigmentation/hyperpigmentation of skin [hp:0007483]
type: SIO_010056
comment: Phenotype [hp:0007483] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Depigmentation/hyperpigmentation of skin
in dataset: phenotype

Limited neck range of motion [hp:0000466]
type: SIO_010056
comment: Phenotype [hp:0000466] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited neck range of motion
in dataset: phenotype

IgM deficiency [hp:0002850]
type: SIO_010056
comment: Phenotype [hp:0002850] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: IgM deficiency
in dataset: phenotype

Decreased renal tubular phosphate excretion [hp:0005572]
type: SIO_010056
comment: Phenotype [hp:0005572] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased renal tubular phosphate excretion
in dataset: phenotype

Generalized papillary lesions [hp:0007482]
type: SIO_010056
comment: Phenotype [hp:0007482] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized papillary lesions
in dataset: phenotype

EMG: neuropathic changes [hp:0003445]
type: SIO_010056
comment: Phenotype [hp:0003445] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EMG: neuropathic changes
in dataset: phenotype

Functional abnormality of the bladder [hp:0000009]
type: SIO_010056
comment: Phenotype [hp:0000009] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Functional abnormality of the bladder
in dataset: phenotype

Lacrimal duct stenosis [hp:0007678]
type: SIO_010056
comment: Phenotype [hp:0007678] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lacrimal duct stenosis
in dataset: phenotype

Ascending aortic dissection [hp:0004933]
type: SIO_010056
comment: Phenotype [hp:0004933] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ascending aortic dissection
in dataset: phenotype

Cervicomedullary schisis [hp:0030325]
type: SIO_010056
comment: Phenotype [hp:0030325] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cervicomedullary schisis
in dataset: phenotype

Type 2 muscle fiber predominance [hp:0010602]
type: SIO_010056
comment: Phenotype [hp:0010602] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type 2 muscle fiber predominance
in dataset: phenotype

Action tremor [hp:0002345]
type: SIO_010056
comment: Phenotype [hp:0002345] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Action tremor
in dataset: phenotype

Portal fibrosis [hp:0006580]
type: SIO_010056
comment: Phenotype [hp:0006580] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Portal fibrosis
in dataset: phenotype

Nonprogressive muscular atrophy [hp:0008964]
type: SIO_010056
comment: Phenotype [hp:0008964] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonprogressive muscular atrophy
in dataset: phenotype

Lung adenocarcinoma [hp:0030078]
type: SIO_010056
comment: Phenotype [hp:0030078] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lung adenocarcinoma
in dataset: phenotype

Webbed neck [hp:0000465]
type: SIO_010056
comment: Phenotype [hp:0000465] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Webbed neck
in dataset: phenotype

3-4 finger syndactyly [hp:0006097]
type: SIO_010056
comment: Phenotype [hp:0006097] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 3-4 finger syndactyly
in dataset: phenotype

Metatarsus adductus [hp:0001840]
type: SIO_010056
comment: Phenotype [hp:0001840] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metatarsus adductus
in dataset: phenotype

Delayed phalangeal epiphyseal ossification [hp:0006016]
type: SIO_010056
comment: Phenotype [hp:0006016] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed phalangeal epiphyseal ossification
in dataset: phenotype

Abnormality of the carpal bones [hp:0001191]
type: SIO_010056
comment: Phenotype [hp:0001191] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the carpal bones
in dataset: phenotype

Glomerulonephritis [hp:0000099]
type: SIO_010056
comment: Phenotype [hp:0000099] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glomerulonephritis
in dataset: phenotype

Adrenocorticotropic hormone deficiency [hp:0011748]
type: SIO_010056
comment: Phenotype [hp:0011748] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenocorticotropic hormone deficiency
in dataset: phenotype

Hyperlipidemia [hp:0003077]
type: SIO_010056
comment: Phenotype [hp:0003077] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperlipidemia
in dataset: phenotype

Contractures of the joints of the lower limbs [hp:0005750]
type: SIO_010056
comment: Phenotype [hp:0005750] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Contractures of the joints of the lower limbs
in dataset: phenotype

Aplasia/Hypoplasia involving the carpal bones [hp:0006502]
type: SIO_010056
comment: Phenotype [hp:0006502] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia involving the carpal bones
in dataset: phenotype

Fibular bowing [hp:0010502]
type: SIO_010056
comment: Phenotype [hp:0010502] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fibular bowing
in dataset: phenotype

Recurrent gram-negative bacterial infections [hp:0005420]
type: SIO_010056
comment: Phenotype [hp:0005420] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent gram-negative bacterial infections
in dataset: phenotype

T-cell acute lymphoblastic leukemias [hp:0006727]
type: SIO_010056
comment: Phenotype [hp:0006727] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: T-cell acute lymphoblastic leukemias
in dataset: phenotype

Vitelliform maculopathy [hp:0007677]
type: SIO_010056
comment: Phenotype [hp:0007677] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vitelliform maculopathy
in dataset: phenotype

Depletion of mitochondrial DNA in liver [hp:0006581]
type: SIO_010056
comment: Phenotype [hp:0006581] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Depletion of mitochondrial DNA in liver
in dataset: phenotype

Intermittent hypothermia [hp:0005964]
type: SIO_010056
comment: Phenotype [hp:0005964] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intermittent hypothermia
in dataset: phenotype

Keratocystic odontogenic tumor [hp:0010603]
type: SIO_010056
comment: Phenotype [hp:0010603] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Keratocystic odontogenic tumor
in dataset: phenotype

Venous varicosities of celiac and mesenteric vessels [hp:0002626]
type: SIO_010056
comment: Phenotype [hp:0002626] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Venous varicosities of celiac and mesenteric vessels
in dataset: phenotype

Exercise-induced muscle stiffness [hp:0008967]
type: SIO_010056
comment: Phenotype [hp:0008967] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exercise-induced muscle stiffness
in dataset: phenotype

Atheroeruptive xanthoma [hp:0001039]
type: SIO_010056
comment: Phenotype [hp:0001039] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atheroeruptive xanthoma
in dataset: phenotype

Bowing of the vocal cords [hp:0008756]
type: SIO_010056
comment: Phenotype [hp:0008756] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bowing of the vocal cords
in dataset: phenotype

Unilateral vertebral artery hypoplasia [hp:0030323]
type: SIO_010056
comment: Phenotype [hp:0030323] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral vertebral artery hypoplasia
in dataset: phenotype

Absence of subcutaneous fat [hp:0007485]
type: SIO_010056
comment: Phenotype [hp:0007485] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of subcutaneous fat
in dataset: phenotype

Preaxial foot polydactyly [hp:0001841]
type: SIO_010056
comment: Phenotype [hp:0001841] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Preaxial foot polydactyly
in dataset: phenotype

Intellectual disability, moderate [hp:0002342]
type: SIO_010056
comment: Phenotype [hp:0002342] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intellectual disability, moderate
in dataset: phenotype

Nonmotile sperm [hp:0012208]
type: SIO_010056
comment: Phenotype [hp:0012208] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonmotile sperm
in dataset: phenotype

Abnormality of the neck [hp:0000464]
type: SIO_010056
comment: Phenotype [hp:0000464] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the neck
in dataset: phenotype

Autosomal recessive inheritance [hp:0000007]
type: SIO_010056
comment: Phenotype [hp:0000007] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autosomal recessive inheritance
in dataset: phenotype

Pulmonary artery atresia [hp:0004935]
type: SIO_010056
comment: Phenotype [hp:0004935] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary artery atresia
in dataset: phenotype

Non-acidotic proximal tubulopathy [hp:0005574]
type: SIO_010056
comment: Phenotype [hp:0005574] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Non-acidotic proximal tubulopathy
in dataset: phenotype

Decreased size of nerve terminals [hp:0003443]
type: SIO_010056
comment: Phenotype [hp:0003443] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased size of nerve terminals
in dataset: phenotype

Wide tufts of distal phalanges [hp:0006095]
type: SIO_010056
comment: Phenotype [hp:0006095] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Wide tufts of distal phalanges
in dataset: phenotype

Aplasia/Hypoplasia of the radius [hp:0006501]
type: SIO_010056
comment: Phenotype [hp:0006501] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the radius
in dataset: phenotype

Decreased serum complement C3 [hp:0005421]
type: SIO_010056
comment: Phenotype [hp:0005421] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased serum complement C3
in dataset: phenotype

Glycosuria [hp:0003076]
type: SIO_010056
comment: Phenotype [hp:0003076] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glycosuria
in dataset: phenotype

Unilateral hypoplasia of pectoralis major muscle [hp:0011959]
type: SIO_010056
comment: Phenotype [hp:0011959] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral hypoplasia of pectoralis major muscle
in dataset: phenotype

Frontotemporal dementia [hp:0002145]
type: SIO_010056
comment: Phenotype [hp:0002145] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontotemporal dementia
in dataset: phenotype

Right aortic arch with mirror image branching [hp:0002627]
type: SIO_010056
comment: Phenotype [hp:0002627] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Right aortic arch with mirror image branching
in dataset: phenotype

Venous malformation [hp:0012721]
type: SIO_010056
comment: Phenotype [hp:0012721] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Venous malformation
in dataset: phenotype

Reye syndrome-like episodes [hp:0006582]
type: SIO_010056
comment: Phenotype [hp:0006582] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reye syndrome-like episodes
in dataset: phenotype

Asymptomatic hyperammonemia [hp:0008162]
type: SIO_010056
comment: Phenotype [hp:0008162] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Asymptomatic hyperammonemia
in dataset: phenotype

Mixed respiratory and metabolic acidosis [hp:0005967]
type: SIO_010056
comment: Phenotype [hp:0005967] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mixed respiratory and metabolic acidosis
in dataset: phenotype

Abnormality of bone mineral density [hp:0004348]
type: SIO_010056
comment: Phenotype [hp:0004348] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of bone mineral density
in dataset: phenotype

Pituitary dwarfism [hp:0000839]
type: SIO_010056
comment: Phenotype [hp:0000839] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pituitary dwarfism
in dataset: phenotype

Congenital giant melanocytic nevus [hp:0005600]
type: SIO_010056
comment: Phenotype [hp:0005600] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital giant melanocytic nevus
in dataset: phenotype

Joint contracture of the hand [hp:0009473]
type: SIO_010056
comment: Phenotype [hp:0009473] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Joint contracture of the hand
in dataset: phenotype

Small forehead [hp:0000350]
type: SIO_010056
comment: Phenotype [hp:0000350] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small forehead
in dataset: phenotype

Depigmented lesions of the retinal pigment epithelium [hp:0008017]
type: SIO_010056
comment: Phenotype [hp:0008017] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Depigmented lesions of the retinal pigment epithelium
in dataset: phenotype

Unilateral vocal cord paralysis [hp:0008757]
type: SIO_010056
comment: Phenotype [hp:0008757] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral vocal cord paralysis
in dataset: phenotype

Normal pressure hydrocephalus [hp:0002343]
type: SIO_010056
comment: Phenotype [hp:0002343] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Normal pressure hydrocephalus
in dataset: phenotype

Neoplasm of the gastrointestinal tract [hp:0007378]
type: SIO_010056
comment: Phenotype [hp:0007378] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the gastrointestinal tract
in dataset: phenotype

Acroosteolysis (feet) [hp:0001842]
type: SIO_010056
comment: Phenotype [hp:0001842] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acroosteolysis (feet)
in dataset: phenotype

Presenile cataracts [hp:0007819]
type: SIO_010056
comment: Phenotype [hp:0007819] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Presenile cataracts
in dataset: phenotype

Anteverted nares [hp:0000463]
type: SIO_010056
comment: Phenotype [hp:0000463] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anteverted nares
in dataset: phenotype

Dental malocclusion [hp:0000689]
type: SIO_010056
comment: Phenotype [hp:0000689] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dental malocclusion
in dataset: phenotype

Juvenile myelomonocytic leukemia [hp:0012209]
type: SIO_010056
comment: Phenotype [hp:0012209] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Juvenile myelomonocytic leukemia
in dataset: phenotype

Alopecia of scalp [hp:0002293]
type: SIO_010056
comment: Phenotype [hp:0002293] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Alopecia of scalp
in dataset: phenotype

Absence of CD8+ T cells [hp:0005422]
type: SIO_010056
comment: Phenotype [hp:0005422] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of CD8+ T cells
in dataset: phenotype

EMG: chronic denervation signs [hp:0003444]
type: SIO_010056
comment: Phenotype [hp:0003444] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EMG: chronic denervation signs
in dataset: phenotype

Abnormality of corneal stroma [hp:0011492]
type: SIO_010056
comment: Phenotype [hp:0011492] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of corneal stroma
in dataset: phenotype

Vascular calcification [hp:0004934]
type: SIO_010056
comment: Phenotype [hp:0004934] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vascular calcification
in dataset: phenotype

Abnormality of female internal genitalia [hp:0000008]
type: SIO_010056
comment: Phenotype [hp:0000008] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of female internal genitalia
in dataset: phenotype

Finger joint hypermobility [hp:0006094]
type: SIO_010056
comment: Phenotype [hp:0006094] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Finger joint hypermobility
in dataset: phenotype

Hemolytic-uremic syndrome [hp:0005575]
type: SIO_010056
comment: Phenotype [hp:0005575] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemolytic-uremic syndrome
in dataset: phenotype

Hypoproteinemia [hp:0003075]
type: SIO_010056
comment: Phenotype [hp:0003075] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoproteinemia
in dataset: phenotype

Coat hanger sign of ribs [hp:0006665]
type: SIO_010056
comment: Phenotype [hp:0006665] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coat hanger sign of ribs
in dataset: phenotype

Aplasia cutis congenita over posterior parietal area [hp:0007590]
type: SIO_010056
comment: Phenotype [hp:0007590] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia cutis congenita over posterior parietal area
in dataset: phenotype

Nevus sebaceous [hp:0010815]
type: SIO_010056
comment: Phenotype [hp:0010815] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nevus sebaceous
in dataset: phenotype

Reduced bone mineral density [hp:0004349]
type: SIO_010056
comment: Phenotype [hp:0004349] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced bone mineral density
in dataset: phenotype

Tethered cord [hp:0002144]
type: SIO_010056
comment: Phenotype [hp:0002144] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tethered cord
in dataset: phenotype

Fatal liver failure in infancy [hp:0006583]
type: SIO_010056
comment: Phenotype [hp:0006583] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fatal liver failure in infancy
in dataset: phenotype

Absent leukocyte alkaline phosphatase [hp:0008161]
type: SIO_010056
comment: Phenotype [hp:0008161] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent leukocyte alkaline phosphatase
in dataset: phenotype

Laryngeal atresia [hp:0008750]
type: SIO_010056
comment: Phenotype [hp:0008750] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laryngeal atresia
in dataset: phenotype

Frontal balding [hp:0002292]
type: SIO_010056
comment: Phenotype [hp:0002292] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontal balding
in dataset: phenotype

Everted lower lip vermilion [hp:0000232]
type: SIO_010056
comment: Phenotype [hp:0000232] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Everted lower lip vermilion
in dataset: phenotype

Abnormalities of placenta or umbilical cord [hp:0001194]
type: SIO_010056
comment: Phenotype [hp:0001194] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormalities of placenta or umbilical cord
in dataset: phenotype

Hyperechogenic kidneys [hp:0004719]
type: SIO_010056
comment: Phenotype [hp:0004719] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperechogenic kidneys
in dataset: phenotype

Leg muscle stiffness [hp:0008969]
type: SIO_010056
comment: Phenotype [hp:0008969] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Leg muscle stiffness
in dataset: phenotype

Glomerulosclerosis [hp:0000096]
type: SIO_010056
comment: Phenotype [hp:0000096] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glomerulosclerosis
in dataset: phenotype

Short 2nd finger [hp:0009536]
type: SIO_010056
comment: Phenotype [hp:0009536] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short 2nd finger
in dataset: phenotype

Glossoptosis [hp:0000162]
type: SIO_010056
comment: Phenotype [hp:0000162] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glossoptosis
in dataset: phenotype

Iritis [hp:0001101]
type: SIO_010056
comment: Phenotype [hp:0001101] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Iritis
in dataset: phenotype

Progressive vitiligo [hp:0005602]
type: SIO_010056
comment: Phenotype [hp:0005602] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive vitiligo
in dataset: phenotype

Mild global developmental delay [hp:0011342]
type: SIO_010056
comment: Phenotype [hp:0011342] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mild global developmental delay
in dataset: phenotype

Dysfunctional alternative complement pathway [hp:0005423]
type: SIO_010056
comment: Phenotype [hp:0005423] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysfunctional alternative complement pathway
in dataset: phenotype

Small intestine carcinoid [hp:0006722]
type: SIO_010056
comment: Phenotype [hp:0006722] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small intestine carcinoid
in dataset: phenotype

Gastrointestinal arteriovenous malformation [hp:0002629]
type: SIO_010056
comment: Phenotype [hp:0002629] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gastrointestinal arteriovenous malformation
in dataset: phenotype

Cold-induced muscle cramps [hp:0003449]
type: SIO_010056
comment: Phenotype [hp:0003449] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cold-induced muscle cramps
in dataset: phenotype

Retroperitoneal fibrosis [hp:0005200]
type: SIO_010056
comment: Phenotype [hp:0005200] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retroperitoneal fibrosis
in dataset: phenotype

Exocrine pancreatic insufficiency [hp:0001738]
type: SIO_010056
comment: Phenotype [hp:0001738] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exocrine pancreatic insufficiency
in dataset: phenotype

Hypoargininemia [hp:0005961]
type: SIO_010056
comment: Phenotype [hp:0005961] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoargininemia
in dataset: phenotype

Abnormality of urine catecholamine concentration [hp:0011281]
type: SIO_010056
comment: Phenotype [hp:0011281] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of urine catecholamine concentration
in dataset: phenotype

Diffuse skin atrophy [hp:0007488]
type: SIO_010056
comment: Phenotype [hp:0007488] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse skin atrophy
in dataset: phenotype

Autosomal dominant inheritance [hp:0000006]
type: SIO_010056
comment: Phenotype [hp:0000006] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autosomal dominant inheritance
in dataset: phenotype

Single umbilical artery [hp:0001195]
type: SIO_010056
comment: Phenotype [hp:0001195] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Single umbilical artery
in dataset: phenotype

Increased proportion of HLA DR+ and CD57+ T cells [hp:0002853]
type: SIO_010056
comment: Phenotype [hp:0002853] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased proportion of HLA DR+ and CD57+ T cells
in dataset: phenotype

Perimembranous ventricular septal defect [hp:0011682]
type: SIO_010056
comment: Phenotype [hp:0011682] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Perimembranous ventricular septal defect
in dataset: phenotype

Laryngeal cleft [hp:0008751]
type: SIO_010056
comment: Phenotype [hp:0008751] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laryngeal cleft
in dataset: phenotype

Spinocerebellar atrophy [hp:0007263]
type: SIO_010056
comment: Phenotype [hp:0007263] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinocerebellar atrophy
in dataset: phenotype

Chemodectoma [hp:0030074]
type: SIO_010056
comment: Phenotype [hp:0030074] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chemodectoma
in dataset: phenotype

Heterochromia iridis [hp:0001100]
type: SIO_010056
comment: Phenotype [hp:0001100] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Heterochromia iridis
in dataset: phenotype

Warfarin-induced skin necrosis [hp:0001038]
type: SIO_010056
comment: Phenotype [hp:0001038] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Warfarin-induced skin necrosis
in dataset: phenotype

Focal seizures without impairment of consciousness or awareness [hp:0002349]
type: SIO_010056
comment: Phenotype [hp:0002349] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Focal seizures without impairment of consciousness or awareness
in dataset: phenotype

Muscle hypertrophy of the lower extremities [hp:0008968]
type: SIO_010056
comment: Phenotype [hp:0008968] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscle hypertrophy of the lower extremities
in dataset: phenotype

Abnormality of the oral cavity [hp:0000163]
type: SIO_010056
comment: Phenotype [hp:0000163] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the oral cavity
in dataset: phenotype

Absent specific antibody response [hp:0005424]
type: SIO_010056
comment: Phenotype [hp:0005424] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent specific antibody response
in dataset: phenotype

Long upper lip [hp:0011341]
type: SIO_010056
comment: Phenotype [hp:0011341] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long upper lip
in dataset: phenotype

Intestinal carcinoid [hp:0006723]
type: SIO_010056
comment: Phenotype [hp:0006723] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intestinal carcinoid
in dataset: phenotype

Cerebellar hemangioblastoma [hp:0006880]
type: SIO_010056
comment: Phenotype [hp:0006880] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebellar hemangioblastoma
in dataset: phenotype

Poliosis [hp:0002290]
type: SIO_010056
comment: Phenotype [hp:0002290] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poliosis
in dataset: phenotype

Symmetric peripheral demyelination [hp:0007262]
type: SIO_010056
comment: Phenotype [hp:0007262] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Symmetric peripheral demyelination
in dataset: phenotype

Abnormality of the nasopharynx [hp:0001739]
type: SIO_010056
comment: Phenotype [hp:0001739] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the nasopharynx
in dataset: phenotype

Abnormality of glycosphingolipid metabolism [hp:0004343]
type: SIO_010056
comment: Phenotype [hp:0004343] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of glycosphingolipid metabolism
in dataset: phenotype

Increased adipose tissue around the neck [hp:0000468]
type: SIO_010056
comment: Phenotype [hp:0000468] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased adipose tissue around the neck
in dataset: phenotype

Severe postnatal growth retardation [hp:0008850]
type: SIO_010056
comment: Phenotype [hp:0008850] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe postnatal growth retardation
in dataset: phenotype

Vitamin D deficiency [hp:0100512]
type: SIO_010056
comment: Phenotype [hp:0100512] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vitamin D deficiency
in dataset: phenotype

Multicystic kidney dysplasia [hp:0000003]
type: SIO_010056
comment: Phenotype [hp:0000003] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multicystic kidney dysplasia
in dataset: phenotype

Diffuse telangiectasia [hp:0007489]
type: SIO_010056
comment: Phenotype [hp:0007489] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse telangiectasia
in dataset: phenotype

Gingivitis [hp:0000230]
type: SIO_010056
comment: Phenotype [hp:0000230] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gingivitis
in dataset: phenotype

Abnormality of the macula [hp:0001103]
type: SIO_010056
comment: Phenotype [hp:0001103] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the macula
in dataset: phenotype

Absent ulna [hp:0003982]
type: SIO_010056
comment: Phenotype [hp:0003982] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent ulna
in dataset: phenotype

Head tremor [hp:0002346]
type: SIO_010056
comment: Phenotype [hp:0002346] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Head tremor
in dataset: phenotype

Narrow mouth [hp:0000160]
type: SIO_010056
comment: Phenotype [hp:0000160] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow mouth
in dataset: phenotype

Tall stature [hp:0000098]
type: SIO_010056
comment: Phenotype [hp:0000098] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tall stature
in dataset: phenotype

Hydropic placenta [hp:0011414]
type: SIO_010056
comment: Phenotype [hp:0011414] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hydropic placenta
in dataset: phenotype

Aplasia of the thymus [hp:0005359]
type: SIO_010056
comment: Phenotype [hp:0005359] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the thymus
in dataset: phenotype

Gait imbalance [hp:0002141]
type: SIO_010056
comment: Phenotype [hp:0002141] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gait imbalance
in dataset: phenotype

Cervical platyspondyly [hp:0004558]
type: SIO_010056
comment: Phenotype [hp:0004558] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cervical platyspondyly
in dataset: phenotype

Hypoplasia of the iris [hp:0007676]
type: SIO_010056
comment: Phenotype [hp:0007676] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the iris
in dataset: phenotype

Severe global developmental delay [hp:0011344]
type: SIO_010056
comment: Phenotype [hp:0011344] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe global developmental delay
in dataset: phenotype

Recurrent sinopulmonary infections [hp:0005425]
type: SIO_010056
comment: Phenotype [hp:0005425] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent sinopulmonary infections
in dataset: phenotype

Adrenocorticotropic hormone excess [hp:0011749]
type: SIO_010056
comment: Phenotype [hp:0011749] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenocorticotropic hormone excess
in dataset: phenotype

Fibular duplication [hp:0010503]
type: SIO_010056
comment: Phenotype [hp:0010503] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fibular duplication
in dataset: phenotype

Carpal bone aplasia [hp:0004231]
type: SIO_010056
comment: Phenotype [hp:0004231] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Carpal bone aplasia
in dataset: phenotype

Recurrent infection of the gastrointestinal tract [hp:0004798]
type: SIO_010056
comment: Phenotype [hp:0004798] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent infection of the gastrointestinal tract
in dataset: phenotype

Arteriosclerosis of small cerebral arteries [hp:0004931]
type: SIO_010056
comment: Phenotype [hp:0004931] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arteriosclerosis of small cerebral arteries
in dataset: phenotype

Anterior creases of earlobe [hp:0009908]
type: SIO_010056
comment: Phenotype [hp:0009908] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior creases of earlobe
in dataset: phenotype

Overlapping toe [hp:0001845]
type: SIO_010056
comment: Phenotype [hp:0001845] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Overlapping toe
in dataset: phenotype

Axonal loss [hp:0003447]
type: SIO_010056
comment: Phenotype [hp:0003447] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Axonal loss
in dataset: phenotype

Aplasia of the epiglottis [hp:0008753]
type: SIO_010056
comment: Phenotype [hp:0008753] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the epiglottis
in dataset: phenotype

Vitamin E deficiency [hp:0100513]
type: SIO_010056
comment: Phenotype [hp:0100513] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vitamin E deficiency
in dataset: phenotype

Neck muscle weakness [hp:0000467]
type: SIO_010056
comment: Phenotype [hp:0000467] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neck muscle weakness
in dataset: phenotype

Ulnar deviation of the hand or of fingers of the hand [hp:0001193]
type: SIO_010056
comment: Phenotype [hp:0001193] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ulnar deviation of the hand or of fingers of the hand
in dataset: phenotype

Increased number of CD4-/CD8- T cells expressing alpha/beta T-cell receptors [hp:0002851]
type: SIO_010056
comment: Phenotype [hp:0002851] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased number of CD4-/CD8- T cells expressing alpha/beta T-cell receptors
in dataset: phenotype

Metacarpophalangeal joint hyperextensibility [hp:0006099]
type: SIO_010056
comment: Phenotype [hp:0006099] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metacarpophalangeal joint hyperextensibility
in dataset: phenotype

Angioid streaks of the retina [hp:0001102]
type: SIO_010056
comment: Phenotype [hp:0001102] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Angioid streaks of the retina
in dataset: phenotype

Median cleft lip [hp:0000161]
type: SIO_010056
comment: Phenotype [hp:0000161] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Median cleft lip
in dataset: phenotype

Focal segmental glomerulosclerosis [hp:0000097]
type: SIO_010056
comment: Phenotype [hp:0000097] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Focal segmental glomerulosclerosis
in dataset: phenotype

Enlarged epiphysis of the middle phalanx of the 3rd finger [hp:0009324]
type: SIO_010056
comment: Phenotype [hp:0009324] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged epiphysis of the middle phalanx of the 3rd finger
in dataset: phenotype

Increased intervertebral space [hp:0030320]
type: SIO_010056
comment: Phenotype [hp:0030320] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased intervertebral space
in dataset: phenotype

Parakeratosis [hp:0001036]
type: SIO_010056
comment: Phenotype [hp:0001036] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Parakeratosis
in dataset: phenotype

Numerous congenital melanocytic nevi [hp:0005603]
type: SIO_010056
comment: Phenotype [hp:0005603] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Numerous congenital melanocytic nevi
in dataset: phenotype

Moderate global developmental delay [hp:0011343]
type: SIO_010056
comment: Phenotype [hp:0011343] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Moderate global developmental delay
in dataset: phenotype

Corneal neovascularization [hp:0011496]
type: SIO_010056
comment: Phenotype [hp:0011496] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corneal neovascularization
in dataset: phenotype

Abnormality of ganglioside metabolism [hp:0004345]
type: SIO_010056
comment: Phenotype [hp:0004345] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of ganglioside metabolism
in dataset: phenotype

Progressive night blindness [hp:0007675]
type: SIO_010056
comment: Phenotype [hp:0007675] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive night blindness
in dataset: phenotype

Pancreatic adenocarcinoma [hp:0006725]
type: SIO_010056
comment: Phenotype [hp:0006725] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pancreatic adenocarcinoma
in dataset: phenotype

Ischemic stroke [hp:0002140]
type: SIO_010056
comment: Phenotype [hp:0002140] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ischemic stroke
in dataset: phenotype

Severe hydrocephalus [hp:0006882]
type: SIO_010056
comment: Phenotype [hp:0006882] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe hydrocephalus
in dataset: phenotype

Persistent hyperplastic primary vitreous [hp:0007968]
type: SIO_010056
comment: Phenotype [hp:0007968] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Persistent hyperplastic primary vitreous
in dataset: phenotype

Accessory carpal bones [hp:0004232]
type: SIO_010056
comment: Phenotype [hp:0004232] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Accessory carpal bones
in dataset: phenotype

Type II lissencephaly [hp:0007260]
type: SIO_010056
comment: Phenotype [hp:0007260] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type II lissencephaly
in dataset: phenotype

Overgrowth [hp:0001548]
type: SIO_010056
comment: Phenotype [hp:0001548] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Overgrowth
in dataset: phenotype

Decreased sensory nerve conduction velocity [hp:0003448]
type: SIO_010056
comment: Phenotype [hp:0003448] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased sensory nerve conduction velocity
in dataset: phenotype

Uplifted earlobe [hp:0009909]
type: SIO_010056
comment: Phenotype [hp:0009909] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Uplifted earlobe
in dataset: phenotype

Increased renal tubular phosphate reabsorption [hp:0005571]
type: SIO_010056
comment: Phenotype [hp:0005571] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased renal tubular phosphate reabsorption
in dataset: phenotype

Defective DNA repair after ultraviolet radiation damage [hp:0003079]
type: SIO_010056
comment: Phenotype [hp:0003079] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Defective DNA repair after ultraviolet radiation damage
in dataset: phenotype

Abnormality of the pulmonary vasculature [hp:0004930]
type: SIO_010056
comment: Phenotype [hp:0004930] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the pulmonary vasculature
in dataset: phenotype

Increased muscle glycogen content [hp:0009051]
type: SIO_010056
comment: Phenotype [hp:0009051] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased muscle glycogen content
in dataset: phenotype

Long hallux [hp:0001847]
type: SIO_010056
comment: Phenotype [hp:0001847] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long hallux
in dataset: phenotype

Salt and pepper retinopathy [hp:0007814]
type: SIO_010056
comment: Phenotype [hp:0007814] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Salt and pepper retinopathy
in dataset: phenotype

Advanced ossification of carpal bones [hp:0004233]
type: SIO_010056
comment: Phenotype [hp:0004233] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Advanced ossification of carpal bones
in dataset: phenotype

Cartilaginous ossification of nose [hp:0005275]
type: SIO_010056
comment: Phenotype [hp:0005275] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cartilaginous ossification of nose
in dataset: phenotype

Epileptic encephalopathy [hp:0200134]
type: SIO_010056
comment: Phenotype [hp:0200134] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Epileptic encephalopathy
in dataset: phenotype

Aplastic clavicles [hp:0006660]
type: SIO_010056
comment: Phenotype [hp:0006660] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplastic clavicles
in dataset: phenotype

Conical incisor [hp:0011065]
type: SIO_010056
comment: Phenotype [hp:0011065] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Conical incisor
in dataset: phenotype

Mydriasis [hp:0011499]
type: SIO_010056
comment: Phenotype [hp:0011499] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mydriasis
in dataset: phenotype

Poikilocytosis [hp:0004447]
type: SIO_010056
comment: Phenotype [hp:0004447] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poikilocytosis
in dataset: phenotype

Abnormal metaphyseal vascular invasion [hp:0003562]
type: SIO_010056
comment: Phenotype [hp:0003562] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal metaphyseal vascular invasion
in dataset: phenotype

Defective B cell differentiation [hp:0005357]
type: SIO_010056
comment: Phenotype [hp:0005357] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Defective B cell differentiation
in dataset: phenotype

Hyperpigmented nevi and streak [hp:0005606]
type: SIO_010056
comment: Phenotype [hp:0005606] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperpigmented nevi and streak
in dataset: phenotype

Retinal atrophy [hp:0001105]
type: SIO_010056
comment: Phenotype [hp:0001105] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal atrophy
in dataset: phenotype

Spastic paraplegia [hp:0001258]
type: SIO_010056
comment: Phenotype [hp:0001258] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spastic paraplegia
in dataset: phenotype

Tubular atrophy [hp:0000092]
type: SIO_010056
comment: Phenotype [hp:0000092] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tubular atrophy
in dataset: phenotype

Streaks of hyperkeratosis along each finger onto the palm [hp:0007501]
type: SIO_010056
comment: Phenotype [hp:0007501] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Streaks of hyperkeratosis along each finger onto the palm
in dataset: phenotype

Absent nipple [hp:0002561]
type: SIO_010056
comment: Phenotype [hp:0002561] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent nipple
in dataset: phenotype

Annular pancreas [hp:0001734]
type: SIO_010056
comment: Phenotype [hp:0001734] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Annular pancreas
in dataset: phenotype

Hepatic failure [hp:0001399]
type: SIO_010056
comment: Phenotype [hp:0001399] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatic failure
in dataset: phenotype

Acute pancreatitis [hp:0001735]
type: SIO_010056
comment: Phenotype [hp:0001735] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute pancreatitis
in dataset: phenotype

Calcaneovalgus deformity [hp:0001848]
type: SIO_010056
comment: Phenotype [hp:0001848] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcaneovalgus deformity
in dataset: phenotype

Nongranulomatous uveitis [hp:0007813]
type: SIO_010056
comment: Phenotype [hp:0007813] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nongranulomatous uveitis
in dataset: phenotype

Quadriceps muscle atrophy [hp:0009050]
type: SIO_010056
comment: Phenotype [hp:0009050] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Quadriceps muscle atrophy
in dataset: phenotype

Decreased serum complement factor I [hp:0005356]
type: SIO_010056
comment: Phenotype [hp:0005356] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased serum complement factor I
in dataset: phenotype

Corpus callosum atrophy [hp:0007371]
type: SIO_010056
comment: Phenotype [hp:0007371] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corpus callosum atrophy
in dataset: phenotype

Membranous cataract [hp:0010922]
type: SIO_010056
comment: Phenotype [hp:0010922] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Membranous cataract
in dataset: phenotype

Fulminant hepatic failure [hp:0004448]
type: SIO_010056
comment: Phenotype [hp:0004448] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fulminant hepatic failure
in dataset: phenotype

Nephronophthisis [hp:0000090]
type: SIO_010056
comment: Phenotype [hp:0000090] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nephronophthisis
in dataset: phenotype

Retrograde ejaculation [hp:0012877]
type: SIO_010056
comment: Phenotype [hp:0012877] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retrograde ejaculation
in dataset: phenotype

Large cafe-au-lait macules with irregular margins [hp:0005605]
type: SIO_010056
comment: Phenotype [hp:0005605] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large cafe-au-lait macules with irregular margins
in dataset: phenotype

Aganglionic megacolon [hp:0002251]
type: SIO_010056
comment: Phenotype [hp:0002251] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aganglionic megacolon
in dataset: phenotype

Hypobetalipoproteinemia [hp:0003563]
type: SIO_010056
comment: Phenotype [hp:0003563] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypobetalipoproteinemia
in dataset: phenotype

Spontaneous esophageal perforation [hp:0005203]
type: SIO_010056
comment: Phenotype [hp:0005203] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spontaneous esophageal perforation
in dataset: phenotype

Drumstick terminal phalanges [hp:0006129]
type: SIO_010056
comment: Phenotype [hp:0006129] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Drumstick terminal phalanges
in dataset: phenotype

Emotional blunting [hp:0030213]
type: SIO_010056
comment: Phenotype [hp:0030213] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Emotional blunting
in dataset: phenotype

Intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material [hp:0006916]
type: SIO_010056
comment: Phenotype [hp:0006916] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material
in dataset: phenotype

Sex-limited autosomal dominant [hp:0001470]
type: SIO_010056
comment: Phenotype [hp:0001470] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sex-limited autosomal dominant
in dataset: phenotype

Macular hypoplasia [hp:0001104]
type: SIO_010056
comment: Phenotype [hp:0001104] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macular hypoplasia
in dataset: phenotype

Abnormality of the renal tubule [hp:0000091]
type: SIO_010056
comment: Phenotype [hp:0000091] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the renal tubule
in dataset: phenotype

Spasticity [hp:0001257]
type: SIO_010056
comment: Phenotype [hp:0001257] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spasticity
in dataset: phenotype

Triphalangeal thumb [hp:0001199]
type: SIO_010056
comment: Phenotype [hp:0001199] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triphalangeal thumb
in dataset: phenotype

Congenital palmoplantar keratodermia [hp:0007597]
type: SIO_010056
comment: Phenotype [hp:0007597] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital palmoplantar keratodermia
in dataset: phenotype

Decreased number of sweat glands [hp:0007500]
type: SIO_010056
comment: Phenotype [hp:0007500] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased number of sweat glands
in dataset: phenotype

Chronic axonal neuropathy [hp:0007267]
type: SIO_010056
comment: Phenotype [hp:0007267] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic axonal neuropathy
in dataset: phenotype

Abnormality of the humeroulnar joint [hp:0100745]
type: SIO_010056
comment: Phenotype [hp:0100745] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the humeroulnar joint
in dataset: phenotype

Abnormality of the fontanelles or cranial sutures [hp:0000235]
type: SIO_010056
comment: Phenotype [hp:0000235] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the fontanelles or cranial sutures
in dataset: phenotype

Absent nasal septal cartilage [hp:0005273]
type: SIO_010056
comment: Phenotype [hp:0005273] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent nasal septal cartilage
in dataset: phenotype

Oligodactyly (feet) [hp:0001849]
type: SIO_010056
comment: Phenotype [hp:0001849] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oligodactyly (feet)
in dataset: phenotype

Aplasia/Hypoplasia of the corpus callosum [hp:0007370]
type: SIO_010056
comment: Phenotype [hp:0007370] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the corpus callosum
in dataset: phenotype

Distal lower limb muscle weakness [hp:0009053]
type: SIO_010056
comment: Phenotype [hp:0009053] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal lower limb muscle weakness
in dataset: phenotype

Macrodactyly of finger [hp:0100746]
type: SIO_010056
comment: Phenotype [hp:0100746] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macrodactyly of finger
in dataset: phenotype

Long nose [hp:0003189]
type: SIO_010056
comment: Phenotype [hp:0003189] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long nose
in dataset: phenotype

Focal necrosis of right ventricular muscle cells [hp:0003338]
type: SIO_010056
comment: Phenotype [hp:0003338] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Focal necrosis of right ventricular muscle cells
in dataset: phenotype

Herpetiform corneal ulceration [hp:0007812]
type: SIO_010056
comment: Phenotype [hp:0007812] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Herpetiform corneal ulceration
in dataset: phenotype

Helicobacter pylori infection [hp:0005202]
type: SIO_010056
comment: Phenotype [hp:0005202] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Helicobacter pylori infection
in dataset: phenotype

Muscular dystrophy [hp:0003560]
type: SIO_010056
comment: Phenotype [hp:0003560] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscular dystrophy
in dataset: phenotype

Constrictive pericarditis [hp:0002563]
type: SIO_010056
comment: Phenotype [hp:0002563] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Constrictive pericarditis
in dataset: phenotype

Bilobate gallbladder [hp:0005608]
type: SIO_010056
comment: Phenotype [hp:0005608] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilobate gallbladder
in dataset: phenotype

Ocular albinism [hp:0001107]
type: SIO_010056
comment: Phenotype [hp:0001107] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ocular albinism
in dataset: phenotype

Dysgerminoma [hp:0100621]
type: SIO_010056
comment: Phenotype [hp:0100621] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysgerminoma
in dataset: phenotype

Irregular dentition [hp:0040079]
type: SIO_010056
comment: Phenotype [hp:0040079] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular dentition
in dataset: phenotype

Abnormality of the inner ear [hp:0000359]
type: SIO_010056
comment: Phenotype [hp:0000359] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the inner ear
in dataset: phenotype

Nephroblastomatosis [hp:0008643]
type: SIO_010056
comment: Phenotype [hp:0008643] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nephroblastomatosis
in dataset: phenotype

Short umbilical cord [hp:0001196]
type: SIO_010056
comment: Phenotype [hp:0001196] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short umbilical cord
in dataset: phenotype

Cerebral dysmyelination [hp:0007266]
type: SIO_010056
comment: Phenotype [hp:0007266] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral dysmyelination
in dataset: phenotype

Bilateral single transverse palmar creases [hp:0007598]
type: SIO_010056
comment: Phenotype [hp:0007598] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral single transverse palmar creases
in dataset: phenotype

Abnormality of the head [hp:0000234]
type: SIO_010056
comment: Phenotype [hp:0000234] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the head
in dataset: phenotype

Prominent nasal tip [hp:0005274]
type: SIO_010056
comment: Phenotype [hp:0005274] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent nasal tip
in dataset: phenotype

Neonatal hypotonia [hp:0001319]
type: SIO_010056
comment: Phenotype [hp:0001319] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neonatal hypotonia
in dataset: phenotype

Absent cellular immunity [hp:0005354]
type: SIO_010056
comment: Phenotype [hp:0005354] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent cellular immunity
in dataset: phenotype

Anomalous splenoportal venous system [hp:0005201]
type: SIO_010056
comment: Phenotype [hp:0005201] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anomalous splenoportal venous system
in dataset: phenotype

Pancreatic cysts [hp:0001737]
type: SIO_010056
comment: Phenotype [hp:0001737] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pancreatic cysts
in dataset: phenotype

Horizontal pendular nystagmus [hp:0007811]
type: SIO_010056
comment: Phenotype [hp:0007811] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Horizontal pendular nystagmus
in dataset: phenotype

Pyrimidine-responsive megaloblastic anemia [hp:0003339]
type: SIO_010056
comment: Phenotype [hp:0003339] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pyrimidine-responsive megaloblastic anemia
in dataset: phenotype

Abnormality of cells of the megakaryocyte lineage [hp:0012143]
type: SIO_010056
comment: Phenotype [hp:0012143] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of cells of the megakaryocyte lineage
in dataset: phenotype

Birth length less than 3rd percentile [hp:0003561]
type: SIO_010056
comment: Phenotype [hp:0003561] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Birth length less than 3rd percentile
in dataset: phenotype

Zonular cataract [hp:0010920]
type: SIO_010056
comment: Phenotype [hp:0010920] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Zonular cataract
in dataset: phenotype

Irregular carpal bones [hp:0004236]
type: SIO_010056
comment: Phenotype [hp:0004236] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular carpal bones
in dataset: phenotype

Impaired distal vibration sensation [hp:0006886]
type: SIO_010056
comment: Phenotype [hp:0006886] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired distal vibration sensation
in dataset: phenotype

Lumbosacral meningocele [hp:0200133]
type: SIO_010056
comment: Phenotype [hp:0200133] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lumbosacral meningocele
in dataset: phenotype

Follicular hyperkeratosis [hp:0007502]
type: SIO_010056
comment: Phenotype [hp:0007502] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Follicular hyperkeratosis
in dataset: phenotype

Triangular shaped distal phalanges of the hand [hp:0009875]
type: SIO_010056
comment: Phenotype [hp:0009875] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular shaped distal phalanges of the hand
in dataset: phenotype

Proteinuria [hp:0000093]
type: SIO_010056
comment: Phenotype [hp:0000093] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proteinuria
in dataset: phenotype

Coma [hp:0001259]
type: SIO_010056
comment: Phenotype [hp:0001259] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coma
in dataset: phenotype

Periorbital hyperpigmentation [hp:0001106]
type: SIO_010056
comment: Phenotype [hp:0001106] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Periorbital hyperpigmentation
in dataset: phenotype

Dermatan sulfate excretion in urine [hp:0008301]
type: SIO_010056
comment: Phenotype [hp:0008301] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dermatan sulfate excretion in urine
in dataset: phenotype

Abnormality of the tracheobronchial system [hp:0005607]
type: SIO_010056
comment: Phenotype [hp:0005607] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the tracheobronchial system
in dataset: phenotype

Diffuse cerebral sclerosis [hp:0006918]
type: SIO_010056
comment: Phenotype [hp:0006918] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse cerebral sclerosis
in dataset: phenotype

Posteriorly rotated ears [hp:0000358]
type: SIO_010056
comment: Phenotype [hp:0000358] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posteriorly rotated ears
in dataset: phenotype

Thin vermilion border [hp:0000233]
type: SIO_010056
comment: Phenotype [hp:0000233] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thin vermilion border
in dataset: phenotype

Low-set nipples [hp:0002562]
type: SIO_010056
comment: Phenotype [hp:0002562] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low-set nipples
in dataset: phenotype

Abnormality of prenatal development or birth [hp:0001197]
type: SIO_010056
comment: Phenotype [hp:0001197] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of prenatal development or birth
in dataset: phenotype

Generalized reticulate brown pigmentation [hp:0007599]
type: SIO_010056
comment: Phenotype [hp:0007599] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized reticulate brown pigmentation
in dataset: phenotype

Secretory diarrhea [hp:0005208]
type: SIO_010056
comment: Phenotype [hp:0005208] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Secretory diarrhea
in dataset: phenotype

Dumbbell-shaped femur [hp:0006375]
type: SIO_010056
comment: Phenotype [hp:0006375] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dumbbell-shaped femur
in dataset: phenotype

Intellectual disability, progressive [hp:0006887]
type: SIO_010056
comment: Phenotype [hp:0006887] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intellectual disability, progressive
in dataset: phenotype

Frontal cortical atrophy [hp:0006913]
type: SIO_010056
comment: Phenotype [hp:0006913] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontal cortical atrophy
in dataset: phenotype

Susceptibility to herpesvirus [hp:0005353]
type: SIO_010056
comment: Phenotype [hp:0005353] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Susceptibility to herpesvirus
in dataset: phenotype

Breast hypoplasia [hp:0003187]
type: SIO_010056
comment: Phenotype [hp:0003187] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Breast hypoplasia
in dataset: phenotype

Muscular edema [hp:0100748]
type: SIO_010056
comment: Phenotype [hp:0100748] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscular edema
in dataset: phenotype

Generalized limb muscle atrophy [hp:0009055]
type: SIO_010056
comment: Phenotype [hp:0009055] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized limb muscle atrophy
in dataset: phenotype

Abnormal enchondral ossification [hp:0003336]
type: SIO_010056
comment: Phenotype [hp:0003336] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal enchondral ossification
in dataset: phenotype

Tubulointerstitial fibrosis [hp:0005576]
type: SIO_010056
comment: Phenotype [hp:0005576] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tubulointerstitial fibrosis
in dataset: phenotype

Progressive hearing impairment [hp:0001730]
type: SIO_010056
comment: Phenotype [hp:0001730] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive hearing impairment
in dataset: phenotype

Loss of subcutaneous adipose tissue from upper limbs [hp:0009056]
type: SIO_010056
comment: Phenotype [hp:0009056] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Loss of subcutaneous adipose tissue from upper limbs
in dataset: phenotype

Adrenal gland agenesis [hp:0011743]
type: SIO_010056
comment: Phenotype [hp:0011743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenal gland agenesis
in dataset: phenotype

Thoracic aortic aneurysm [hp:0012727]
type: SIO_010056
comment: Phenotype [hp:0012727] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thoracic aortic aneurysm
in dataset: phenotype

Subungual hyperkeratotic fragments [hp:0008410]
type: SIO_010056
comment: Phenotype [hp:0008410] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subungual hyperkeratotic fragments
in dataset: phenotype

Progressive hyperpigmentation [hp:0007505]
type: SIO_010056
comment: Phenotype [hp:0007505] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive hyperpigmentation
in dataset: phenotype

Arteriovenous malformation [hp:0100026]
type: SIO_010056
comment: Phenotype [hp:0100026] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arteriovenous malformation
in dataset: phenotype

Congenital myopia [hp:0008012]
type: SIO_010056
comment: Phenotype [hp:0008012] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital myopia
in dataset: phenotype

Lethargy [hp:0001254]
type: SIO_010056
comment: Phenotype [hp:0001254] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lethargy
in dataset: phenotype

Midface prominence [hp:0012371]
type: SIO_010056
comment: Phenotype [hp:0012371] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Midface prominence
in dataset: phenotype

Molar tooth sign on MRI [hp:0002419]
type: SIO_010056
comment: Phenotype [hp:0002419] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Molar tooth sign on MRI
in dataset: phenotype

Meningoencephalocele [hp:0006888]
type: SIO_010056
comment: Phenotype [hp:0006888] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Meningoencephalocele
in dataset: phenotype

Temperature instability [hp:0005968]
type: SIO_010056
comment: Phenotype [hp:0005968] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Temperature instability
in dataset: phenotype

Dentinogenesis imperfecta limited to primary teeth [hp:0011060]
type: SIO_010056
comment: Phenotype [hp:0011060] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dentinogenesis imperfecta limited to primary teeth
in dataset: phenotype

Reduced prothrombin consumption [hp:0003337]
type: SIO_010056
comment: Phenotype [hp:0003337] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced prothrombin consumption
in dataset: phenotype

Inverted nipples [hp:0003186]
type: SIO_010056
comment: Phenotype [hp:0003186] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inverted nipples
in dataset: phenotype

Chest pain [hp:0100749]
type: SIO_010056
comment: Phenotype [hp:0100749] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chest pain
in dataset: phenotype

Large fontanelles [hp:0000239]
type: SIO_010056
comment: Phenotype [hp:0000239] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large fontanelles
in dataset: phenotype

Aplasia/Hypoplastia of the eccrine sweat glands [hp:0007592]
type: SIO_010056
comment: Phenotype [hp:0007592] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplastia of the eccrine sweat glands
in dataset: phenotype

Horizontal supranuclear gaze palsy [hp:0007817]
type: SIO_010056
comment: Phenotype [hp:0007817] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Horizontal supranuclear gaze palsy
in dataset: phenotype

Prominent nasolabial fold [hp:0005272]
type: SIO_010056
comment: Phenotype [hp:0005272] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent nasolabial fold
in dataset: phenotype

Scapuloperoneal myopathy [hp:0009054]
type: SIO_010056
comment: Phenotype [hp:0009054] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scapuloperoneal myopathy
in dataset: phenotype

Severe T-cell immunodeficiency [hp:0005352]
type: SIO_010056
comment: Phenotype [hp:0005352] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe T-cell immunodeficiency
in dataset: phenotype

Axonal degeneration [hp:0040078]
type: SIO_010056
comment: Phenotype [hp:0040078] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Axonal degeneration
in dataset: phenotype

Aplasia/Hypoplasia of the 3rd toe [hp:0010331]
type: SIO_010056
comment: Phenotype [hp:0010331] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the 3rd toe
in dataset: phenotype

Abnormality of the outer ear [hp:0000356]
type: SIO_010056
comment: Phenotype [hp:0000356] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the outer ear
in dataset: phenotype

Brittle hair [hp:0002299]
type: SIO_010056
comment: Phenotype [hp:0002299] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Brittle hair
in dataset: phenotype

Gallbladder dysfunction [hp:0005609]
type: SIO_010056
comment: Phenotype [hp:0005609] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gallbladder dysfunction
in dataset: phenotype

Aplasia/Hypoplasia of the phalanges of the hand [hp:0009767]
type: SIO_010056
comment: Phenotype [hp:0009767] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the phalanges of the hand
in dataset: phenotype

Peripheral opacification of the cornea [hp:0008011]
type: SIO_010056
comment: Phenotype [hp:0008011] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral opacification of the cornea
in dataset: phenotype

Malformation of the heart and great vessels [hp:0002564]
type: SIO_010056
comment: Phenotype [hp:0002564] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malformation of the heart and great vessels
in dataset: phenotype

Diffuse slow skin atrophy [hp:0007504]
type: SIO_010056
comment: Phenotype [hp:0007504] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse slow skin atrophy
in dataset: phenotype

Overfriendliness [hp:0100025]
type: SIO_010056
comment: Phenotype [hp:0100025] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Overfriendliness
in dataset: phenotype

Inability to walk by childhood/adolescence [hp:0006915]
type: SIO_010056
comment: Phenotype [hp:0006915] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inability to walk by childhood/adolescence
in dataset: phenotype

Intermittent diarrhea [hp:0002254]
type: SIO_010056
comment: Phenotype [hp:0002254] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intermittent diarrhea
in dataset: phenotype

Hypersexuality [hp:0030214]
type: SIO_010056
comment: Phenotype [hp:0030214] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypersexuality
in dataset: phenotype

Pancreatic pseudocyst [hp:0005206]
type: SIO_010056
comment: Phenotype [hp:0005206] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pancreatic pseudocyst
in dataset: phenotype

Intellectual disability, borderline [hp:0006889]
type: SIO_010056
comment: Phenotype [hp:0006889] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intellectual disability, borderline
in dataset: phenotype

Abnormal cartilage collagen [hp:0008271]
type: SIO_010056
comment: Phenotype [hp:0008271] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal cartilage collagen
in dataset: phenotype

Oral-pharyngeal dysphagia [hp:0200136]
type: SIO_010056
comment: Phenotype [hp:0200136] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oral-pharyngeal dysphagia
in dataset: phenotype

Short sacroiliac notch [hp:0003185]
type: SIO_010056
comment: Phenotype [hp:0003185] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short sacroiliac notch
in dataset: phenotype

Elevated circulating catecholamine level [hp:0003334]
type: SIO_010056
comment: Phenotype [hp:0003334] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated circulating catecholamine level
in dataset: phenotype

Generalized tonic seizures [hp:0010818]
type: SIO_010056
comment: Phenotype [hp:0010818] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized tonic seizures
in dataset: phenotype

Decreased sweating due to autonomic dysfunction [hp:0007480]
type: SIO_010056
comment: Phenotype [hp:0007480] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased sweating due to autonomic dysfunction
in dataset: phenotype

Broad phalanges of the hand [hp:0009768]
type: SIO_010056
comment: Phenotype [hp:0009768] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad phalanges of the hand
in dataset: phenotype

Hydrocephalus [hp:0000238]
type: SIO_010056
comment: Phenotype [hp:0000238] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hydrocephalus
in dataset: phenotype

Abnormality of the pancreas [hp:0001732]
type: SIO_010056
comment: Phenotype [hp:0001732] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the pancreas
in dataset: phenotype

Increased muscle lipid content [hp:0009058]
type: SIO_010056
comment: Phenotype [hp:0009058] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased muscle lipid content
in dataset: phenotype

Hypopituitarism [hp:0040075]
type: SIO_010056
comment: Phenotype [hp:0040075] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypopituitarism
in dataset: phenotype

Intellectual disability, mild [hp:0001256]
type: SIO_010056
comment: Phenotype [hp:0001256] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intellectual disability, mild
in dataset: phenotype

Narrow nose [hp:0000460]
type: SIO_010056
comment: Phenotype [hp:0000460] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow nose
in dataset: phenotype

Ectopic thyroid [hp:0100028]
type: SIO_010056
comment: Phenotype [hp:0100028] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopic thyroid
in dataset: phenotype

Cutaneous syndactyly [hp:0012725]
type: SIO_010056
comment: Phenotype [hp:0012725] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cutaneous syndactyly
in dataset: phenotype

Limited elbow flexion [hp:0006376]
type: SIO_010056
comment: Phenotype [hp:0006376] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited elbow flexion
in dataset: phenotype

Colonic diverticulosis [hp:0002253]
type: SIO_010056
comment: Phenotype [hp:0002253] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Colonic diverticulosis
in dataset: phenotype

Impaired reabsorption of chloride [hp:0005579]
type: SIO_010056
comment: Phenotype [hp:0005579] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired reabsorption of chloride
in dataset: phenotype

Low gonadotropins (secondary hypogonadism) [hp:0003335]
type: SIO_010056
comment: Phenotype [hp:0003335] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low gonadotropins (secondary hypogonadism)
in dataset: phenotype

Decreased hip abduction [hp:0003184]
type: SIO_010056
comment: Phenotype [hp:0003184] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased hip abduction
in dataset: phenotype

Reduced quantity of Von Willebrand factor [hp:0012147]
type: SIO_010056
comment: Phenotype [hp:0012147] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced quantity of Von Willebrand factor
in dataset: phenotype

Atonic seizures [hp:0010819]
type: SIO_010056
comment: Phenotype [hp:0010819] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atonic seizures
in dataset: phenotype

Bullet-shaped phalanges of the hand [hp:0009769]
type: SIO_010056
comment: Phenotype [hp:0009769] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bullet-shaped phalanges of the hand
in dataset: phenotype

Small anterior fontanelle [hp:0000237]
type: SIO_010056
comment: Phenotype [hp:0000237] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small anterior fontanelle
in dataset: phenotype

Red hair [hp:0002297]
type: SIO_010056
comment: Phenotype [hp:0002297] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Red hair
in dataset: phenotype

Pancreatitis [hp:0001733]
type: SIO_010056
comment: Phenotype [hp:0001733] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pancreatitis
in dataset: phenotype

Redundant skin in infancy [hp:0007595]
type: SIO_010056
comment: Phenotype [hp:0007595] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Redundant skin in infancy
in dataset: phenotype

Spinal muscular atrophy [hp:0007269]
type: SIO_010056
comment: Phenotype [hp:0007269] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinal muscular atrophy
in dataset: phenotype

Cortical gyral simplification [hp:0009879]
type: SIO_010056
comment: Phenotype [hp:0009879] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cortical gyral simplification
in dataset: phenotype

Calf muscle hypoplasia [hp:0008962]
type: SIO_010056
comment: Phenotype [hp:0008962] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calf muscle hypoplasia
in dataset: phenotype

Intestinal malrotation [hp:0002566]
type: SIO_010056
comment: Phenotype [hp:0002566] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intestinal malrotation
in dataset: phenotype

Neonatal short-trunk short stature [hp:0008857]
type: SIO_010056
comment: Phenotype [hp:0008857] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neonatal short-trunk short stature
in dataset: phenotype

Recurrent pancreatitis [hp:0100027]
type: SIO_010056
comment: Phenotype [hp:0100027] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent pancreatitis
in dataset: phenotype

Long proximal phalanx of finger [hp:0006127]
type: SIO_010056
comment: Phenotype [hp:0006127] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long proximal phalanx of finger
in dataset: phenotype

Phimosis [hp:0001741]
type: SIO_010056
comment: Phenotype [hp:0001741] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Phimosis
in dataset: phenotype

Cleft ala nasi [hp:0003191]
type: SIO_010056
comment: Phenotype [hp:0003191] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cleft ala nasi
in dataset: phenotype

Degeneration of the striatum [hp:0040140]
type: SIO_010056
comment: Phenotype [hp:0040140] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Degeneration of the striatum
in dataset: phenotype

Optic nerve coloboma [hp:0000588]
type: SIO_010056
comment: Phenotype [hp:0000588] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Optic nerve coloboma
in dataset: phenotype

Myocardial fibrosis [hp:0001685]
type: SIO_010056
comment: Phenotype [hp:0001685] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myocardial fibrosis
in dataset: phenotype

Ataxia [hp:0001251]
type: SIO_010056
comment: Phenotype [hp:0001251] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ataxia
in dataset: phenotype

Esophageal neoplasm [hp:0100751]
type: SIO_010056
comment: Phenotype [hp:0100751] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Esophageal neoplasm
in dataset: phenotype

Limited elbow movement [hp:0002996]
type: SIO_010056
comment: Phenotype [hp:0002996] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited elbow movement
in dataset: phenotype

Delayed closure of the anterior fontanelle [hp:0001476]
type: SIO_010056
comment: Phenotype [hp:0001476] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed closure of the anterior fontanelle
in dataset: phenotype

Absent thumb [hp:0009777]
type: SIO_010056
comment: Phenotype [hp:0009777] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent thumb
in dataset: phenotype

Enlarged peripheral nerve [hp:0012645]
type: SIO_010056
comment: Phenotype [hp:0012645] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged peripheral nerve
in dataset: phenotype

Infantile hypercalcemia [hp:0008250]
type: SIO_010056
comment: Phenotype [hp:0008250] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Infantile hypercalcemia
in dataset: phenotype

Edema [hp:0000969]
type: SIO_010056
comment: Phenotype [hp:0000969] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Edema
in dataset: phenotype

Calcific stippling of infantile cartilaginous skeleton [hp:0005841]
type: SIO_010056
comment: Phenotype [hp:0005841] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcific stippling of infantile cartilaginous skeleton
in dataset: phenotype

Hypoplasia of proximal fibula [hp:0006442]
type: SIO_010056
comment: Phenotype [hp:0006442] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of proximal fibula
in dataset: phenotype

Forearm reduction defects [hp:0006368]
type: SIO_010056
comment: Phenotype [hp:0006368] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Forearm reduction defects
in dataset: phenotype

Prolonged brainstem auditory evoked potentials [hp:0004466]
type: SIO_010056
comment: Phenotype [hp:0004466] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolonged brainstem auditory evoked potentials
in dataset: phenotype

Abnormal EKG [hp:0003115]
type: SIO_010056
comment: Phenotype [hp:0003115] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal EKG
in dataset: phenotype

Chronic rhinitis [hp:0002257]
type: SIO_010056
comment: Phenotype [hp:0002257] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic rhinitis
in dataset: phenotype

Recurrent upper and lower respiratory tract infections [hp:0200117]
type: SIO_010056
comment: Phenotype [hp:0200117] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent upper and lower respiratory tract infections
in dataset: phenotype

Widening of cervical spinal canal [hp:0004571]
type: SIO_010056
comment: Phenotype [hp:0004571] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Widening of cervical spinal canal
in dataset: phenotype

Diffuse mesangial sclerosis [hp:0001967]
type: SIO_010056
comment: Phenotype [hp:0001967] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse mesangial sclerosis
in dataset: phenotype

Ketonuria [hp:0002919]
type: SIO_010056
comment: Phenotype [hp:0002919] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ketonuria
in dataset: phenotype

Aminoaciduria [hp:0003355]
type: SIO_010056
comment: Phenotype [hp:0003355] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aminoaciduria
in dataset: phenotype

Abnormality of the voice [hp:0001608]
type: SIO_010056
comment: Phenotype [hp:0001608] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the voice
in dataset: phenotype

Tardive dyskinesia [hp:0040141]
type: SIO_010056
comment: Phenotype [hp:0040141] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tardive dyskinesia
in dataset: phenotype

Coloboma [hp:0000589]
type: SIO_010056
comment: Phenotype [hp:0000589] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coloboma
in dataset: phenotype

Atelectasis [hp:0100750]
type: SIO_010056
comment: Phenotype [hp:0100750] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atelectasis
in dataset: phenotype

Muscular hypotonia [hp:0001252]
type: SIO_010056
comment: Phenotype [hp:0001252] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscular hypotonia
in dataset: phenotype

Loss of voice [hp:0001686]
type: SIO_010056
comment: Phenotype [hp:0001686] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Loss of voice
in dataset: phenotype

Impaired vibratory sensation [hp:0002495]
type: SIO_010056
comment: Phenotype [hp:0002495] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired vibratory sensation
in dataset: phenotype

Abnormality of the ulna [hp:0002997]
type: SIO_010056
comment: Phenotype [hp:0002997] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the ulna
in dataset: phenotype

Male-limited autosomal dominant [hp:0001475]
type: SIO_010056
comment: Phenotype [hp:0001475] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Male-limited autosomal dominant
in dataset: phenotype

Adactyly [hp:0009776]
type: SIO_010056
comment: Phenotype [hp:0009776] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adactyly
in dataset: phenotype

Skeletal myopathy [hp:0003756]
type: SIO_010056
comment: Phenotype [hp:0003756] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skeletal myopathy
in dataset: phenotype

Conspicuously happy disposition [hp:0100024]
type: SIO_010056
comment: Phenotype [hp:0100024] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Conspicuously happy disposition
in dataset: phenotype

Congenital goiter [hp:0008251]
type: SIO_010056
comment: Phenotype [hp:0008251] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital goiter
in dataset: phenotype

Limb dysmetria [hp:0002406]
type: SIO_010056
comment: Phenotype [hp:0002406] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb dysmetria
in dataset: phenotype

Hyperthreoninemia [hp:0003354]
type: SIO_010056
comment: Phenotype [hp:0003354] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperthreoninemia
in dataset: phenotype

1-5 toe syndactyly [hp:0010713]
type: SIO_010056
comment: Phenotype [hp:0010713] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 1-5 toe syndactyly
in dataset: phenotype

Ectodermal dysplasia [hp:0000968]
type: SIO_010056
comment: Phenotype [hp:0000968] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectodermal dysplasia
in dataset: phenotype

Testicular seminoma [hp:0100617]
type: SIO_010056
comment: Phenotype [hp:0100617] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Testicular seminoma
in dataset: phenotype

Distal ileal atresia [hp:0200116]
type: SIO_010056
comment: Phenotype [hp:0200116] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal ileal atresia
in dataset: phenotype

Irido-fundal coloboma [hp:0007748]
type: SIO_010056
comment: Phenotype [hp:0007748] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irido-fundal coloboma
in dataset: phenotype

Hypermagnesemia [hp:0002918]
type: SIO_010056
comment: Phenotype [hp:0002918] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypermagnesemia
in dataset: phenotype

Subglottic stenosis [hp:0001607]
type: SIO_010056
comment: Phenotype [hp:0001607] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subglottic stenosis
in dataset: phenotype

Allergic rhinitis [hp:0003193]
type: SIO_010056
comment: Phenotype [hp:0003193] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Allergic rhinitis
in dataset: phenotype

Mesangial abnormality [hp:0001966]
type: SIO_010056
comment: Phenotype [hp:0001966] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mesangial abnormality
in dataset: phenotype

Increased vertebral height [hp:0004570]
type: SIO_010056
comment: Phenotype [hp:0004570] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased vertebral height
in dataset: phenotype

Decreased glucosephosphate isomerase activity [hp:0003568]
type: SIO_010056
comment: Phenotype [hp:0003568] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased glucosephosphate isomerase activity
in dataset: phenotype

Cerebral palsy [hp:0100021]
type: SIO_010056
comment: Phenotype [hp:0100021] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral palsy
in dataset: phenotype

Hypoglycemic coma [hp:0001325]
type: SIO_010056
comment: Phenotype [hp:0001325] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoglycemic coma
in dataset: phenotype

Abnormality of the scalp [hp:0001965]
type: SIO_010056
comment: Phenotype [hp:0001965] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the scalp
in dataset: phenotype

5-oxoprolinase deficiency [hp:0040142]
type: SIO_010056
comment: Phenotype [hp:0040142] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 5-oxoprolinase deficiency
in dataset: phenotype

Neurofibrosarcoma [hp:0100697]
type: SIO_010056
comment: Phenotype [hp:0100697] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neurofibrosarcoma
in dataset: phenotype

Positive Romberg sign [hp:0002403]
type: SIO_010056
comment: Phenotype [hp:0002403] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Positive Romberg sign
in dataset: phenotype

Large basal ganglia [hp:0007048]
type: SIO_010056
comment: Phenotype [hp:0007048] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large basal ganglia
in dataset: phenotype

Type 1 fibers relatively smaller than type 2 fibers [hp:0003755]
type: SIO_010056
comment: Phenotype [hp:0003755] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type 1 fibers relatively smaller than type 2 fibers
in dataset: phenotype

Upper airway obstruction [hp:0002781]
type: SIO_010056
comment: Phenotype [hp:0002781] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Upper airway obstruction
in dataset: phenotype

Progressive extrapyramidal movement disorder [hp:0007153]
type: SIO_010056
comment: Phenotype [hp:0007153] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive extrapyramidal movement disorder
in dataset: phenotype

Amniotic constriction ring [hp:0009775]
type: SIO_010056
comment: Phenotype [hp:0009775] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Amniotic constriction ring
in dataset: phenotype

Absent left hemidiaphragm [hp:0009112]
type: SIO_010056
comment: Phenotype [hp:0009112] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent left hemidiaphragm
in dataset: phenotype

Broad distal phalanges of all fingers [hp:0009880]
type: SIO_010056
comment: Phenotype [hp:0009880] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad distal phalanges of all fingers
in dataset: phenotype

Increased density of long bone diaphyses [hp:0006440]
type: SIO_010056
comment: Phenotype [hp:0006440] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased density of long bone diaphyses
in dataset: phenotype

Hypochloremia [hp:0003113]
type: SIO_010056
comment: Phenotype [hp:0003113] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypochloremia
in dataset: phenotype

Thymic hormone decreased [hp:0003357]
type: SIO_010056
comment: Phenotype [hp:0003357] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thymic hormone decreased
in dataset: phenotype

Hypomagnesemia [hp:0002917]
type: SIO_010056
comment: Phenotype [hp:0002917] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypomagnesemia
in dataset: phenotype

Short nasal bridge [hp:0003194]
type: SIO_010056
comment: Phenotype [hp:0003194] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short nasal bridge
in dataset: phenotype

Acute hepatitis [hp:0200119]
type: SIO_010056
comment: Phenotype [hp:0200119] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute hepatitis
in dataset: phenotype

Vocal cord paralysis (caused by tumor impingement) [hp:0001606]
type: SIO_010056
comment: Phenotype [hp:0001606] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vocal cord paralysis (caused by tumor impingement)
in dataset: phenotype

Postauricular pit [hp:0004464]
type: SIO_010056
comment: Phenotype [hp:0004464] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Postauricular pit
in dataset: phenotype

Conjunctivitis [hp:0000509]
type: SIO_010056
comment: Phenotype [hp:0000509] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Conjunctivitis
in dataset: phenotype

Sinus bradycardia [hp:0001688]
type: SIO_010056
comment: Phenotype [hp:0001688] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sinus bradycardia
in dataset: phenotype

Elevated leukocyte alkaline phosphatase [hp:0008318]
type: SIO_010056
comment: Phenotype [hp:0008318] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated leukocyte alkaline phosphatase
in dataset: phenotype

Patellar dislocation [hp:0002999]
type: SIO_010056
comment: Phenotype [hp:0002999] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Patellar dislocation
in dataset: phenotype

Compensatory chin elevation [hp:0001477]
type: SIO_010056
comment: Phenotype [hp:0001477] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Compensatory chin elevation
in dataset: phenotype

Subcutaneous neurofibromas [hp:0100698]
type: SIO_010056
comment: Phenotype [hp:0100698] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subcutaneous neurofibromas
in dataset: phenotype

Seizures [hp:0001250]
type: SIO_010056
comment: Phenotype [hp:0001250] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Seizures
in dataset: phenotype

Aplasia/Hypoplasia of metatarsal bones [hp:0001964]
type: SIO_010056
comment: Phenotype [hp:0001964] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of metatarsal bones
in dataset: phenotype

Muscle weakness [hp:0001324]
type: SIO_010056
comment: Phenotype [hp:0001324] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscle weakness
in dataset: phenotype

Abnormality of movement [hp:0100022]
type: SIO_010056
comment: Phenotype [hp:0100022] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of movement
in dataset: phenotype

Thickened superior cerebellar peduncle [hp:0002404]
type: SIO_010056
comment: Phenotype [hp:0002404] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thickened superior cerebellar peduncle
in dataset: phenotype

Atrophy of the dentate nucleus [hp:0007047]
type: SIO_010056
comment: Phenotype [hp:0007047] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atrophy of the dentate nucleus
in dataset: phenotype

Short distal phalanx of finger [hp:0009882]
type: SIO_010056
comment: Phenotype [hp:0009882] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short distal phalanx of finger
in dataset: phenotype

Bronchomalacia [hp:0002780]
type: SIO_010056
comment: Phenotype [hp:0002780] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bronchomalacia
in dataset: phenotype

Diaphragmatic weakness [hp:0009113]
type: SIO_010056
comment: Phenotype [hp:0009113] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diaphragmatic weakness
in dataset: phenotype

Spastic ataxia [hp:0002497]
type: SIO_010056
comment: Phenotype [hp:0002497] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spastic ataxia
in dataset: phenotype

Patchy hypo- and hyperpigmentation [hp:0007509]
type: SIO_010056
comment: Phenotype [hp:0007509] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Patchy hypo- and hyperpigmentation
in dataset: phenotype

Crumpled long bones [hp:0006367]
type: SIO_010056
comment: Phenotype [hp:0006367] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Crumpled long bones
in dataset: phenotype

Premature calcification of mitral annulus [hp:0005136]
type: SIO_010056
comment: Phenotype [hp:0005136] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature calcification of mitral annulus
in dataset: phenotype

Abnormality of chromosome segregation [hp:0002916]
type: SIO_010056
comment: Phenotype [hp:0002916] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of chromosome segregation
in dataset: phenotype

Abdominal colic [hp:0011848]
type: SIO_010056
comment: Phenotype [hp:0011848] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abdominal colic
in dataset: phenotype

Absent brainstem auditory responses [hp:0004463]
type: SIO_010056
comment: Phenotype [hp:0004463] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent brainstem auditory responses
in dataset: phenotype

Ptosis [hp:0000508]
type: SIO_010056
comment: Phenotype [hp:0000508] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ptosis
in dataset: phenotype

Ovarian neoplasm [hp:0100615]
type: SIO_010056
comment: Phenotype [hp:0100615] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ovarian neoplasm
in dataset: phenotype

Vocal cord paralysis [hp:0001605]
type: SIO_010056
comment: Phenotype [hp:0001605] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vocal cord paralysis
in dataset: phenotype

Malabsorption of Vitamin B12 [hp:0200118]
type: SIO_010056
comment: Phenotype [hp:0200118] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malabsorption of Vitamin B12
in dataset: phenotype

Duplication of the distal phalanx of hand [hp:0009883]
type: SIO_010056
comment: Phenotype [hp:0009883] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Duplication of the distal phalanx of hand
in dataset: phenotype

Familial predisposition [hp:0001472]
type: SIO_010056
comment: Phenotype [hp:0001472] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Familial predisposition
in dataset: phenotype

Pseudohypoparathyroidism [hp:0000852]
type: SIO_010056
comment: Phenotype [hp:0000852] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pseudohypoparathyroidism
in dataset: phenotype

Stroke-like episodes [hp:0002401]
type: SIO_010056
comment: Phenotype [hp:0002401] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stroke-like episodes
in dataset: phenotype

Symphalangism affecting the phalanges of the hand [hp:0009773]
type: SIO_010056
comment: Phenotype [hp:0009773] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Symphalangism affecting the phalanges of the hand
in dataset: phenotype

Transient neonatal diabetes mellitus [hp:0008255]
type: SIO_010056
comment: Phenotype [hp:0008255] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Transient neonatal diabetes mellitus
in dataset: phenotype

Abnormality of the tibia [hp:0002992]
type: SIO_010056
comment: Phenotype [hp:0002992] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the tibia
in dataset: phenotype

Abnormal speech discrimination [hp:0001963]
type: SIO_010056
comment: Phenotype [hp:0001963] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal speech discrimination
in dataset: phenotype

Iris coloboma [hp:0000612]
type: SIO_010056
comment: Phenotype [hp:0000612] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Iris coloboma
in dataset: phenotype

Abnormality of the corticospinal tract [hp:0002492]
type: SIO_010056
comment: Phenotype [hp:0002492] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the corticospinal tract
in dataset: phenotype

Aplasia/Hypoplasia of the colon [hp:0100811]
type: SIO_010056
comment: Phenotype [hp:0100811] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the colon
in dataset: phenotype

Recurrent lower respiratory tract infections [hp:0002783]
type: SIO_010056
comment: Phenotype [hp:0002783] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent lower respiratory tract infections
in dataset: phenotype

Myositis [hp:0100614]
type: SIO_010056
comment: Phenotype [hp:0100614] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myositis
in dataset: phenotype

Elevated erythrocyte sedimentation rate [hp:0003565]
type: SIO_010056
comment: Phenotype [hp:0003565] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated erythrocyte sedimentation rate
in dataset: phenotype

Dysplastic patella [hp:0006446]
type: SIO_010056
comment: Phenotype [hp:0006446] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysplastic patella
in dataset: phenotype

Thin glomerular basement membrane [hp:0012577]
type: SIO_010056
comment: Phenotype [hp:0012577] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thin glomerular basement membrane
in dataset: phenotype

Prolonged bleeding after dental extraction [hp:0006298]
type: SIO_010056
comment: Phenotype [hp:0006298] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolonged bleeding after dental extraction
in dataset: phenotype

EKG: T-wave abnormalities [hp:0005135]
type: SIO_010056
comment: Phenotype [hp:0005135] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EKG: T-wave abnormalities
in dataset: phenotype

Decreased circulating renin level [hp:0003351]
type: SIO_010056
comment: Phenotype [hp:0003351] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased circulating renin level
in dataset: phenotype

Cutis marmorata [hp:0000965]
type: SIO_010056
comment: Phenotype [hp:0000965] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cutis marmorata
in dataset: phenotype

Eczema [hp:0000964]
type: SIO_010056
comment: Phenotype [hp:0000964] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Eczema
in dataset: phenotype

Congenital hypothyroidism [hp:0000851]
type: SIO_010056
comment: Phenotype [hp:0000851] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital hypothyroidism
in dataset: phenotype

Agenesis of maxillary lateral incisor [hp:0000690]
type: SIO_010056
comment: Phenotype [hp:0000690] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Agenesis of maxillary lateral incisor
in dataset: phenotype

Tapered distal phalanges of finger [hp:0009884]
type: SIO_010056
comment: Phenotype [hp:0009884] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tapered distal phalanges of finger
in dataset: phenotype

Patchy sclerosis of finger phalanx [hp:0009772]
type: SIO_010056
comment: Phenotype [hp:0009772] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Patchy sclerosis of finger phalanx
in dataset: phenotype

Adrenocortical adenoma [hp:0008256]
type: SIO_010056
comment: Phenotype [hp:0008256] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenocortical adenoma
in dataset: phenotype

Spasticity of facial muscles [hp:0002491]
type: SIO_010056
comment: Phenotype [hp:0002491] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spasticity of facial muscles
in dataset: phenotype

Vertebral clefting [hp:0008428]
type: SIO_010056
comment: Phenotype [hp:0008428] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vertebral clefting
in dataset: phenotype

EEG with irregular generalized spike and wave complexes [hp:0001326]
type: SIO_010056
comment: Phenotype [hp:0001326] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EEG with irregular generalized spike and wave complexes
in dataset: phenotype

Choroid coloboma [hp:0000611]
type: SIO_010056
comment: Phenotype [hp:0000611] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Choroid coloboma
in dataset: phenotype

Palpitations [hp:0001962]
type: SIO_010056
comment: Phenotype [hp:0001962] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palpitations
in dataset: phenotype

Death in early adulthood [hp:0100613]
type: SIO_010056
comment: Phenotype [hp:0100613] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Death in early adulthood
in dataset: phenotype

Short distal phalanx of the 3rd finger [hp:0004180]
type: SIO_010056
comment: Phenotype [hp:0004180] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short distal phalanx of the 3rd finger
in dataset: phenotype

Band keratopathy [hp:0000585]
type: SIO_010056
comment: Phenotype [hp:0000585] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Band keratopathy
in dataset: phenotype

Mania [hp:0100754]
type: SIO_010056
comment: Phenotype [hp:0100754] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mania
in dataset: phenotype

Abnormal mitochondria in muscle tissue [hp:0008316]
type: SIO_010056
comment: Phenotype [hp:0008316] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal mitochondria in muscle tissue
in dataset: phenotype

Hyperchloridura [hp:0002914]
type: SIO_010056
comment: Phenotype [hp:0002914] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperchloridura
in dataset: phenotype

Abnormality of urine homeostasis [hp:0003110]
type: SIO_010056
comment: Phenotype [hp:0003110] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of urine homeostasis
in dataset: phenotype

Folate-dependent fragile site at Xq28 [hp:0003564]
type: SIO_010056
comment: Phenotype [hp:0003564] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Folate-dependent fragile site at Xq28
in dataset: phenotype

Lens luxation [hp:0012019]
type: SIO_010056
comment: Phenotype [hp:0012019] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lens luxation
in dataset: phenotype

Telecanthus [hp:0000506]
type: SIO_010056
comment: Phenotype [hp:0000506] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Telecanthus
in dataset: phenotype

Hypoplasia of dental enamel [hp:0006297]
type: SIO_010056
comment: Phenotype [hp:0006297] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of dental enamel
in dataset: phenotype

Membranous nephropathy [hp:0012578]
type: SIO_010056
comment: Phenotype [hp:0012578] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Membranous nephropathy
in dataset: phenotype

Absence of the pulmonary valve [hp:0005134]
type: SIO_010056
comment: Phenotype [hp:0005134] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of the pulmonary valve
in dataset: phenotype

Chronic bronchitis [hp:0004469]
type: SIO_010056
comment: Phenotype [hp:0004469] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic bronchitis
in dataset: phenotype

Abnormality of cells of the lymphoid lineage [hp:0012140]
type: SIO_010056
comment: Phenotype [hp:0012140] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of cells of the lymphoid lineage
in dataset: phenotype

Metaphyseal spurs [hp:0005054]
type: SIO_010056
comment: Phenotype [hp:0005054] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metaphyseal spurs
in dataset: phenotype

Diaphragmatic eventration [hp:0009110]
type: SIO_010056
comment: Phenotype [hp:0009110] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diaphragmatic eventration
in dataset: phenotype

Iridodonesis [hp:0100693]
type: SIO_010056
comment: Phenotype [hp:0100693] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Iridodonesis
in dataset: phenotype

Osteolytic defects of the phalanges of the hand [hp:0009771]
type: SIO_010056
comment: Phenotype [hp:0009771] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteolytic defects of the phalanges of the hand
in dataset: phenotype

Microdontia [hp:0000691]
type: SIO_010056
comment: Phenotype [hp:0000691] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microdontia
in dataset: phenotype

Anterolateral radial head dislocation [hp:0005050]
type: SIO_010056
comment: Phenotype [hp:0005050] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterolateral radial head dislocation
in dataset: phenotype

Thyroid adenoma [hp:0000854]
type: SIO_010056
comment: Phenotype [hp:0000854] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thyroid adenoma
in dataset: phenotype

Impaired epinephrine-induced platelet aggregation [hp:0008148]
type: SIO_010056
comment: Phenotype [hp:0008148] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired epinephrine-induced platelet aggregation
in dataset: phenotype

Decreased plasma free carnitine [hp:0008315]
type: SIO_010056
comment: Phenotype [hp:0008315] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased plasma free carnitine
in dataset: phenotype

Schizophrenia [hp:0100753]
type: SIO_010056
comment: Phenotype [hp:0100753] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Schizophrenia
in dataset: phenotype

Sclerotic scapulae [hp:0001474]
type: SIO_010056
comment: Phenotype [hp:0001474] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sclerotic scapulae
in dataset: phenotype

Abnormal rapid eye movement (REM) sleep [hp:0002494]
type: SIO_010056
comment: Phenotype [hp:0002494] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal rapid eye movement (REM) sleep
in dataset: phenotype

Shallow orbits [hp:0000586]
type: SIO_010056
comment: Phenotype [hp:0000586] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shallow orbits
in dataset: phenotype

Hypoplastic heart [hp:0001961]
type: SIO_010056
comment: Phenotype [hp:0001961] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic heart
in dataset: phenotype

Odontogenic neoplasm [hp:0100612]
type: SIO_010056
comment: Phenotype [hp:0100612] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Odontogenic neoplasm
in dataset: phenotype

Bronchiolitis [hp:0011950]
type: SIO_010056
comment: Phenotype [hp:0011950] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bronchiolitis
in dataset: phenotype

Aplasia cutis congenita on trunk or limbs [hp:0007589]
type: SIO_010056
comment: Phenotype [hp:0007589] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia cutis congenita on trunk or limbs
in dataset: phenotype

Visual impairment [hp:0000505]
type: SIO_010056
comment: Phenotype [hp:0000505] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Visual impairment
in dataset: phenotype

Myoglobinuria [hp:0002913]
type: SIO_010056
comment: Phenotype [hp:0002913] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myoglobinuria
in dataset: phenotype

Microspherocytosis [hp:0004835]
type: SIO_010056
comment: Phenotype [hp:0004835] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microspherocytosis
in dataset: phenotype

Abnormal renal physiology [hp:0012211]
type: SIO_010056
comment: Phenotype [hp:0012211] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal renal physiology
in dataset: phenotype

Limited mobility of proximal interphalangeal joint [hp:0006217]
type: SIO_010056
comment: Phenotype [hp:0006217] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited mobility of proximal interphalangeal joint
in dataset: phenotype

Anomalous tracheal cartilage [hp:0004468]
type: SIO_010056
comment: Phenotype [hp:0004468] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anomalous tracheal cartilage
in dataset: phenotype

Petechiae [hp:0000967]
type: SIO_010056
comment: Phenotype [hp:0000967] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Petechiae
in dataset: phenotype

Right ventricular dilatation [hp:0005133]
type: SIO_010056
comment: Phenotype [hp:0005133] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Right ventricular dilatation
in dataset: phenotype

Propionyl-CoA carboxylase deficiency [hp:0003353]
type: SIO_010056
comment: Phenotype [hp:0003353] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Propionyl-CoA carboxylase deficiency
in dataset: phenotype

Ovotestis [hp:0012861]
type: SIO_010056
comment: Phenotype [hp:0012861] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ovotestis
in dataset: phenotype

Hypoplasia of lymphatic vessels [hp:0003759]
type: SIO_010056
comment: Phenotype [hp:0003759] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of lymphatic vessels
in dataset: phenotype

Trichorrhexis nodosa [hp:0009886]
type: SIO_010056
comment: Phenotype [hp:0009886] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Trichorrhexis nodosa
in dataset: phenotype

Reduced subcutaneous adipose tissue [hp:0003758]
type: SIO_010056
comment: Phenotype [hp:0003758] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced subcutaneous adipose tissue
in dataset: phenotype

Metatarsal osteolysis [hp:0001473]
type: SIO_010056
comment: Phenotype [hp:0001473] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metatarsal osteolysis
in dataset: phenotype

Decreased activity of mitochondrial complex II [hp:0008314]
type: SIO_010056
comment: Phenotype [hp:0008314] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased activity of mitochondrial complex II
in dataset: phenotype

Goiter [hp:0000853]
type: SIO_010056
comment: Phenotype [hp:0000853] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Goiter
in dataset: phenotype

Misalignment of teeth [hp:0000692]
type: SIO_010056
comment: Phenotype [hp:0000692] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Misalignment of teeth
in dataset: phenotype

Hypokalemic metabolic alkalosis [hp:0001960]
type: SIO_010056
comment: Phenotype [hp:0001960] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypokalemic metabolic alkalosis
in dataset: phenotype

Upper motor neuron dysfunction [hp:0002493]
type: SIO_010056
comment: Phenotype [hp:0002493] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Upper motor neuron dysfunction
in dataset: phenotype

Multiple glomerular cysts [hp:0100611]
type: SIO_010056
comment: Phenotype [hp:0100611] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple glomerular cysts
in dataset: phenotype

Pointed helix [hp:0100810]
type: SIO_010056
comment: Phenotype [hp:0100810] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pointed helix
in dataset: phenotype

Abnormal liver lobulation [hp:0100752]
type: SIO_010056
comment: Phenotype [hp:0100752] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal liver lobulation
in dataset: phenotype

Reticular hyperpigmentation [hp:0007588]
type: SIO_010056
comment: Phenotype [hp:0007588] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reticular hyperpigmentation
in dataset: phenotype

Abnormality of the optic nerve [hp:0000587]
type: SIO_010056
comment: Phenotype [hp:0000587] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the optic nerve
in dataset: phenotype

Tibial torsion [hp:0100694]
type: SIO_010056
comment: Phenotype [hp:0100694] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tibial torsion
in dataset: phenotype

Specific learning disability [hp:0001328]
type: SIO_010056
comment: Phenotype [hp:0001328] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Specific learning disability
in dataset: phenotype

Abnormality of vision [hp:0000504]
type: SIO_010056
comment: Phenotype [hp:0000504] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of vision
in dataset: phenotype

Abnormality of hair texture [hp:0010719]
type: SIO_010056
comment: Phenotype [hp:0010719] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of hair texture
in dataset: phenotype

Hoarse voice [hp:0001609]
type: SIO_010056
comment: Phenotype [hp:0001609] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hoarse voice
in dataset: phenotype

Increased serum prostaglandin E2 [hp:0003566]
type: SIO_010056
comment: Phenotype [hp:0003566] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased serum prostaglandin E2
in dataset: phenotype

Abnormal renal morphology [hp:0012210]
type: SIO_010056
comment: Phenotype [hp:0012210] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal renal morphology
in dataset: phenotype

Acute promyelocytic leukemia [hp:0004836]
type: SIO_010056
comment: Phenotype [hp:0004836] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute promyelocytic leukemia
in dataset: phenotype

Progressive bifocal chorioretinal atrophy [hp:0007810]
type: SIO_010056
comment: Phenotype [hp:0007810] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive bifocal chorioretinal atrophy
in dataset: phenotype

Methylmalonic acidemia [hp:0002912]
type: SIO_010056
comment: Phenotype [hp:0002912] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Methylmalonic acidemia
in dataset: phenotype

Pancreatic squamous cell carcinoma [hp:0012142]
type: SIO_010056
comment: Phenotype [hp:0012142] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pancreatic squamous cell carcinoma
in dataset: phenotype

Decreased serum leptin [hp:0003292]
type: SIO_010056
comment: Phenotype [hp:0003292] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased serum leptin
in dataset: phenotype

Pericardial constriction [hp:0005132]
type: SIO_010056
comment: Phenotype [hp:0005132] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pericardial constriction
in dataset: phenotype

Hypohidrosis [hp:0000966]
type: SIO_010056
comment: Phenotype [hp:0000966] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypohidrosis
in dataset: phenotype

Preauricular pit [hp:0004467]
type: SIO_010056
comment: Phenotype [hp:0004467] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Preauricular pit
in dataset: phenotype

Endopolyploidy on chromosome studies of bone marrow [hp:0003352]
type: SIO_010056
comment: Phenotype [hp:0003352] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Endopolyploidy on chromosome studies of bone marrow
in dataset: phenotype

Patellar aplasia [hp:0006443]
type: SIO_010056
comment: Phenotype [hp:0006443] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Patellar aplasia
in dataset: phenotype

Colorectal polyposis [hp:0200063]
type: SIO_010056
comment: Phenotype [hp:0200063] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Colorectal polyposis
in dataset: phenotype

Acute lymphatic leukemia [hp:0006721]
type: SIO_010056
comment: Phenotype [hp:0006721] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute lymphatic leukemia
in dataset: phenotype

Chronic lymphocytic meningitis [hp:0007041]
type: SIO_010056
comment: Phenotype [hp:0007041] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic lymphocytic meningitis
in dataset: phenotype

Recurrent bacterial skin infections [hp:0005406]
type: SIO_010056
comment: Phenotype [hp:0005406] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent bacterial skin infections
in dataset: phenotype

Slender distal phalanx of finger [hp:0012296]
type: SIO_010056
comment: Phenotype [hp:0012296] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slender distal phalanx of finger
in dataset: phenotype

Short tibia [hp:0005736]
type: SIO_010056
comment: Phenotype [hp:0005736] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short tibia
in dataset: phenotype

Onset [hp:0003674]
type: SIO_010056
comment: Phenotype [hp:0003674] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Onset
in dataset: phenotype

Degenerative vitreoretinopathy [hp:0007964]
type: SIO_010056
comment: Phenotype [hp:0007964] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Degenerative vitreoretinopathy
in dataset: phenotype

Breast carcinoma [hp:0003002]
type: SIO_010056
comment: Phenotype [hp:0003002] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Breast carcinoma
in dataset: phenotype

Decreased glomerular filtration rate [hp:0012213]
type: SIO_010056
comment: Phenotype [hp:0012213] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased glomerular filtration rate
in dataset: phenotype

Metopic suture patent to nasal root [hp:0005495]
type: SIO_010056
comment: Phenotype [hp:0005495] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metopic suture patent to nasal root
in dataset: phenotype

Female pseudohermaphroditism [hp:0010458]
type: SIO_010056
comment: Phenotype [hp:0010458] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Female pseudohermaphroditism
in dataset: phenotype

Skin tags [hp:0010609]
type: SIO_010056
comment: Phenotype [hp:0010609] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skin tags
in dataset: phenotype

Tortuosity of conjunctival vessels [hp:0000503]
type: SIO_010056
comment: Phenotype [hp:0000503] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tortuosity of conjunctival vessels
in dataset: phenotype

Miosis [hp:0000616]
type: SIO_010056
comment: Phenotype [hp:0000616] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Miosis
in dataset: phenotype

Tracheal calcification [hp:0002787]
type: SIO_010056
comment: Phenotype [hp:0002787] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tracheal calcification
in dataset: phenotype

Abnormality of T cells [hp:0002843]
type: SIO_010056
comment: Phenotype [hp:0002843] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of T cells
in dataset: phenotype

Abnormality of the larynx [hp:0001600]
type: SIO_010056
comment: Phenotype [hp:0001600] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the larynx
in dataset: phenotype

Absent distal interphalangeal creases [hp:0001032]
type: SIO_010056
comment: Phenotype [hp:0001032] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent distal interphalangeal creases
in dataset: phenotype

Parathyroid hyperplasia [hp:0008208]
type: SIO_010056
comment: Phenotype [hp:0008208] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Parathyroid hyperplasia
in dataset: phenotype

Triangular epiphysis of the middle phalanx of the 2nd finger [hp:0009523]
type: SIO_010056
comment: Phenotype [hp:0009523] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular epiphysis of the middle phalanx of the 2nd finger
in dataset: phenotype

Adrenocorticotropin (ACTH) receptor (ACTHR) defect [hp:0008259]
type: SIO_010056
comment: Phenotype [hp:0008259] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenocorticotropin (ACTH) receptor (ACTHR) defect
in dataset: phenotype

Cyanosis [hp:0000961]
type: SIO_010056
comment: Phenotype [hp:0000961] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cyanosis
in dataset: phenotype

Pigmentary retinopathy [hp:0000580]
type: SIO_010056
comment: Phenotype [hp:0000580] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pigmentary retinopathy
in dataset: phenotype

Impaired proprioception [hp:0010831]
type: SIO_010056
comment: Phenotype [hp:0010831] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired proprioception
in dataset: phenotype

IgA deposition in the glomerulus [hp:0000794]
type: SIO_010056
comment: Phenotype [hp:0000794] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: IgA deposition in the glomerulus
in dataset: phenotype

Low-to-normal blood pressure [hp:0002632]
type: SIO_010056
comment: Phenotype [hp:0002632] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low-to-normal blood pressure
in dataset: phenotype

Nasal polyposis [hp:0100582]
type: SIO_010056
comment: Phenotype [hp:0100582] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nasal polyposis
in dataset: phenotype

Long eyelashes in irregular rows [hp:0007740]
type: SIO_010056
comment: Phenotype [hp:0007740] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long eyelashes in irregular rows
in dataset: phenotype

Slender proximal phalanx of finger [hp:0012297]
type: SIO_010056
comment: Phenotype [hp:0012297] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slender proximal phalanx of finger
in dataset: phenotype

Insulin resistance [hp:0000855]
type: SIO_010056
comment: Phenotype [hp:0000855] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Insulin resistance
in dataset: phenotype

Single interphalangeal crease of fifth finger [hp:0006216]
type: SIO_010056
comment: Phenotype [hp:0006216] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Single interphalangeal crease of fifth finger
in dataset: phenotype

Absence of visual evoked potentials [hp:0007965]
type: SIO_010056
comment: Phenotype [hp:0007965] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of visual evoked potentials
in dataset: phenotype

Glomus jugular tumor [hp:0003001]
type: SIO_010056
comment: Phenotype [hp:0003001] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glomus jugular tumor
in dataset: phenotype

Abnormality of the pupil [hp:0000615]
type: SIO_010056
comment: Phenotype [hp:0000615] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the pupil
in dataset: phenotype

True hermaphroditism [hp:0010459]
type: SIO_010056
comment: Phenotype [hp:0010459] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: True hermaphroditism
in dataset: phenotype

Lip hyperpigmentation [hp:0100816]
type: SIO_010056
comment: Phenotype [hp:0100816] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lip hyperpigmentation
in dataset: phenotype

Cleft at the superior portion of the pinna [hp:0008537]
type: SIO_010056
comment: Phenotype [hp:0008537] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cleft at the superior portion of the pinna
in dataset: phenotype

Abnormality of the conjunctiva [hp:0000502]
type: SIO_010056
comment: Phenotype [hp:0000502] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the conjunctiva
in dataset: phenotype

Slender build [hp:0001533]
type: SIO_010056
comment: Phenotype [hp:0001533] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slender build
in dataset: phenotype

Acute tubulointerstitial nephritis [hp:0004729]
type: SIO_010056
comment: Phenotype [hp:0004729] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute tubulointerstitial nephritis
in dataset: phenotype

Subcutaneous lipoma [hp:0001031]
type: SIO_010056
comment: Phenotype [hp:0001031] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subcutaneous lipoma
in dataset: phenotype

Tracheobronchomalacia [hp:0002786]
type: SIO_010056
comment: Phenotype [hp:0002786] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tracheobronchomalacia
in dataset: phenotype

Shell teeth [hp:0000694]
type: SIO_010056
comment: Phenotype [hp:0000694] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shell teeth
in dataset: phenotype

Primary adrenal insufficiency [hp:0008207]
type: SIO_010056
comment: Phenotype [hp:0008207] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Primary adrenal insufficiency
in dataset: phenotype

Elevated hepatic transaminases [hp:0002910]
type: SIO_010056
comment: Phenotype [hp:0002910] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated hepatic transaminases
in dataset: phenotype

Blepharophimosis [hp:0000581]
type: SIO_010056
comment: Phenotype [hp:0000581] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Blepharophimosis
in dataset: phenotype

Corneal perforation [hp:0100583]
type: SIO_010056
comment: Phenotype [hp:0100583] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corneal perforation
in dataset: phenotype

Ascending aortic aneurysm [hp:0002631]
type: SIO_010056
comment: Phenotype [hp:0002631] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ascending aortic aneurysm
in dataset: phenotype

Abnormality of the urethra [hp:0000795]
type: SIO_010056
comment: Phenotype [hp:0000795] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the urethra
in dataset: phenotype

Abnormality of the teeth [hp:0000164]
type: SIO_010056
comment: Phenotype [hp:0000164] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the teeth
in dataset: phenotype

Sacral dimple [hp:0000960]
type: SIO_010056
comment: Phenotype [hp:0000960] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sacral dimple
in dataset: phenotype

Thin proximal phalanges with broad epiphyses of the hand [hp:0006213]
type: SIO_010056
comment: Phenotype [hp:0006213] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thin proximal phalanges with broad epiphyses of the hand
in dataset: phenotype

Spina bifida occulta at L5 [hp:0004601]
type: SIO_010056
comment: Phenotype [hp:0004601] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spina bifida occulta at L5
in dataset: phenotype

Menstrual irregularities [hp:0000858]
type: SIO_010056
comment: Phenotype [hp:0000858] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Menstrual irregularities
in dataset: phenotype

Respiratory distress [hp:0002098]
type: SIO_010056
comment: Phenotype [hp:0002098] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Respiratory distress
in dataset: phenotype

Choroidoretinal degeneration [hp:0200065]
type: SIO_010056
comment: Phenotype [hp:0200065] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Choroidoretinal degeneration
in dataset: phenotype

Increase in B cell number [hp:0005404]
type: SIO_010056
comment: Phenotype [hp:0005404] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increase in B cell number
in dataset: phenotype

Elevated 8-dehydrocholesterol [hp:0003462]
type: SIO_010056
comment: Phenotype [hp:0003462] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated 8-dehydrocholesterol
in dataset: phenotype

Testicular microlithiasis [hp:0012215]
type: SIO_010056
comment: Phenotype [hp:0012215] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Testicular microlithiasis
in dataset: phenotype

Abnormality of the nasolacrimal system [hp:0000614]
type: SIO_010056
comment: Phenotype [hp:0000614] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the nasolacrimal system
in dataset: phenotype

Testicular torsion [hp:0100813]
type: SIO_010056
comment: Phenotype [hp:0100813] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Testicular torsion
in dataset: phenotype

Progressive disorder [hp:0003676]
type: SIO_010056
comment: Phenotype [hp:0003676] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive disorder
in dataset: phenotype

Ivory epiphyses of the phalanges of the hand [hp:0010234]
type: SIO_010056
comment: Phenotype [hp:0010234] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ivory epiphyses of the phalanges of the hand
in dataset: phenotype

Natal tooth [hp:0000695]
type: SIO_010056
comment: Phenotype [hp:0000695] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Natal tooth
in dataset: phenotype

Glaucoma [hp:0000501]
type: SIO_010056
comment: Phenotype [hp:0000501] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glaucoma
in dataset: phenotype

Increased number of peripheral CD3+ T cells [hp:0002845]
type: SIO_010056
comment: Phenotype [hp:0002845] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased number of peripheral CD3+ T cells
in dataset: phenotype

Increased CSF lactate [hp:0002490]
type: SIO_010056
comment: Phenotype [hp:0002490] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased CSF lactate
in dataset: phenotype

Hydroxyprolinuria [hp:0003080]
type: SIO_010056
comment: Phenotype [hp:0003080] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hydroxyprolinuria
in dataset: phenotype

Tachypnea [hp:0002789]
type: SIO_010056
comment: Phenotype [hp:0002789] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tachypnea
in dataset: phenotype

Flattening of the talar dome [hp:0008144]
type: SIO_010056
comment: Phenotype [hp:0008144] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flattening of the talar dome
in dataset: phenotype

Fat malabsorption [hp:0002630]
type: SIO_010056
comment: Phenotype [hp:0002630] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fat malabsorption
in dataset: phenotype

Fibular aplasia [hp:0002990]
type: SIO_010056
comment: Phenotype [hp:0002990] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fibular aplasia
in dataset: phenotype

Thin skin [hp:0000963]
type: SIO_010056
comment: Phenotype [hp:0000963] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thin skin
in dataset: phenotype

Upslanted palpebral fissure [hp:0000582]
type: SIO_010056
comment: Phenotype [hp:0000582] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Upslanted palpebral fissure
in dataset: phenotype

Hypermelanotic macule [hp:0001034]
type: SIO_010056
comment: Phenotype [hp:0001034] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypermelanotic macule
in dataset: phenotype

Depigmented fundus [hp:0007680]
type: SIO_010056
comment: Phenotype [hp:0007680] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Depigmented fundus
in dataset: phenotype

Neonatal insulin-dependent diabetes mellitus [hp:0000857]
type: SIO_010056
comment: Phenotype [hp:0000857] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neonatal insulin-dependent diabetes mellitus
in dataset: phenotype

Emphysema [hp:0002097]
type: SIO_010056
comment: Phenotype [hp:0002097] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Emphysema
in dataset: phenotype

Sclerotic vertebral endplates [hp:0004576]
type: SIO_010056
comment: Phenotype [hp:0004576] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sclerotic vertebral endplates
in dataset: phenotype

Increased urinary O-linked sialopeptides [hp:0003461]
type: SIO_010056
comment: Phenotype [hp:0003461] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased urinary O-linked sialopeptides
in dataset: phenotype

T lymphocytopenia [hp:0005403]
type: SIO_010056
comment: Phenotype [hp:0005403] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: T lymphocytopenia
in dataset: phenotype

Cervical vertebral fusion (C2/C3) [hp:0004602]
type: SIO_010056
comment: Phenotype [hp:0004602] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cervical vertebral fusion (C2/C3)
in dataset: phenotype

Midline skin dimples over anterior/posterior fontanelles [hp:0005498]
type: SIO_010056
comment: Phenotype [hp:0005498] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Midline skin dimples over anterior/posterior fontanelles
in dataset: phenotype

Photophobia [hp:0000613]
type: SIO_010056
comment: Phenotype [hp:0000613] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Photophobia
in dataset: phenotype

Long distal phalanx of finger [hp:0012299]
type: SIO_010056
comment: Phenotype [hp:0012299] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long distal phalanx of finger
in dataset: phenotype

Delayed eruption of permanent teeth [hp:0000696]
type: SIO_010056
comment: Phenotype [hp:0000696] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed eruption of permanent teeth
in dataset: phenotype

Vitamin B12 deficiency [hp:0100502]
type: SIO_010056
comment: Phenotype [hp:0100502] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vitamin B12 deficiency
in dataset: phenotype

Facial flushing after alcohol intake [hp:0001033]
type: SIO_010056
comment: Phenotype [hp:0001033] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial flushing after alcohol intake
in dataset: phenotype

Impaired renal concentrating ability [hp:0004727]
type: SIO_010056
comment: Phenotype [hp:0004727] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired renal concentrating ability
in dataset: phenotype

Teleangiectasia of the skin [hp:0100585]
type: SIO_010056
comment: Phenotype [hp:0100585] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Teleangiectasia of the skin
in dataset: phenotype

Increased urinary potassium [hp:0003081]
type: SIO_010056
comment: Phenotype [hp:0003081] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased urinary potassium
in dataset: phenotype

Congenital nonbullous ichthyosiform erythroderma [hp:0007479]
type: SIO_010056
comment: Phenotype [hp:0007479] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital nonbullous ichthyosiform erythroderma
in dataset: phenotype

Recurrent upper respiratory tract infections [hp:0002788]
type: SIO_010056
comment: Phenotype [hp:0002788] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent upper respiratory tract infections
in dataset: phenotype

Severe periodontitis [hp:0000166]
type: SIO_010056
comment: Phenotype [hp:0000166] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe periodontitis
in dataset: phenotype

Abnormality of the fibula [hp:0002991]
type: SIO_010056
comment: Phenotype [hp:0002991] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the fibula
in dataset: phenotype

Coarctation of aorta [hp:0001680]
type: SIO_010056
comment: Phenotype [hp:0001680] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coarctation of aorta
in dataset: phenotype

Insulin-dependent but ketosis-resistant diabetes [hp:0008205]
type: SIO_010056
comment: Phenotype [hp:0008205] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Insulin-dependent but ketosis-resistant diabetes
in dataset: phenotype

Congenital adrenal hyperplasia [hp:0008258]
type: SIO_010056
comment: Phenotype [hp:0008258] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital adrenal hyperplasia
in dataset: phenotype

Hyperkeratosis [hp:0000962]
type: SIO_010056
comment: Phenotype [hp:0000962] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperkeratosis
in dataset: phenotype

Calcium nephrolithiasis [hp:0004724]
type: SIO_010056
comment: Phenotype [hp:0004724] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcium nephrolithiasis
in dataset: phenotype

Vocal cord paresis [hp:0001604]
type: SIO_010056
comment: Phenotype [hp:0001604] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vocal cord paresis
in dataset: phenotype

Hypophosphatemia [hp:0002148]
type: SIO_010056
comment: Phenotype [hp:0002148] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypophosphatemia
in dataset: phenotype

Rapidly progressive [hp:0003678]
type: SIO_010056
comment: Phenotype [hp:0003678] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rapidly progressive
in dataset: phenotype

Intestinal fistula [hp:0100819]
type: SIO_010056
comment: Phenotype [hp:0100819] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intestinal fistula
in dataset: phenotype

Impaired memory B-cell generation [hp:0002847]
type: SIO_010056
comment: Phenotype [hp:0002847] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired memory B-cell generation
in dataset: phenotype

Dislocated radial head [hp:0003083]
type: SIO_010056
comment: Phenotype [hp:0003083] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dislocated radial head
in dataset: phenotype

Abnormal cholesterol homeostasis [hp:0003464]
type: SIO_010056
comment: Phenotype [hp:0003464] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal cholesterol homeostasis
in dataset: phenotype

Recurrent spontaneous abortion [hp:0200067]
type: SIO_010056
comment: Phenotype [hp:0200067] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent spontaneous abortion
in dataset: phenotype

Neuroblastoma [hp:0003006]
type: SIO_010056
comment: Phenotype [hp:0003006] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neuroblastoma
in dataset: phenotype

Microtia, first degree [hp:0011266]
type: SIO_010056
comment: Phenotype [hp:0011266] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microtia, first degree
in dataset: phenotype

Anterior beaking of lower thoracic vertebrae [hp:0004607]
type: SIO_010056
comment: Phenotype [hp:0004607] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior beaking of lower thoracic vertebrae
in dataset: phenotype

Fluctuations in consciousness [hp:0007159]
type: SIO_010056
comment: Phenotype [hp:0007159] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fluctuations in consciousness
in dataset: phenotype

Angina pectoris [hp:0001681]
type: SIO_010056
comment: Phenotype [hp:0001681] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Angina pectoris
in dataset: phenotype

Acetabular spurs [hp:0010454]
type: SIO_010056
comment: Phenotype [hp:0010454] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acetabular spurs
in dataset: phenotype

Aseptic leukocyturia [hp:0100586]
type: SIO_010056
comment: Phenotype [hp:0100586] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aseptic leukocyturia
in dataset: phenotype

Crumpled ear [hp:0009901]
type: SIO_010056
comment: Phenotype [hp:0009901] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Crumpled ear
in dataset: phenotype

Hematuria [hp:0000790]
type: SIO_010056
comment: Phenotype [hp:0000790] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hematuria
in dataset: phenotype

Gingival fibromatosis [hp:0000169]
type: SIO_010056
comment: Phenotype [hp:0000169] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gingival fibromatosis
in dataset: phenotype

Scarring [hp:0100699]
type: SIO_010056
comment: Phenotype [hp:0100699] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scarring
in dataset: phenotype

L-2-hydroxyglutaric aciduria [hp:0040144]
type: SIO_010056
comment: Phenotype [hp:0040144] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: L-2-hydroxyglutaric aciduria
in dataset: phenotype

Slow progression [hp:0003677]
type: SIO_010056
comment: Phenotype [hp:0003677] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slow progression
in dataset: phenotype

Synovial sarcoma [hp:0012570]
type: SIO_010056
comment: Phenotype [hp:0012570] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Synovial sarcoma
in dataset: phenotype

Impaired convergence [hp:0000619]
type: SIO_010056
comment: Phenotype [hp:0000619] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired convergence
in dataset: phenotype

Nonprogressive visual loss [hp:0200068]
type: SIO_010056
comment: Phenotype [hp:0200068] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonprogressive visual loss
in dataset: phenotype

Hyperuricemia [hp:0002149]
type: SIO_010056
comment: Phenotype [hp:0002149] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperuricemia
in dataset: phenotype

Fractures of the long bones [hp:0003084]
type: SIO_010056
comment: Phenotype [hp:0003084] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fractures of the long bones
in dataset: phenotype

Specific anti-polysaccharide antibody deficiency [hp:0002848]
type: SIO_010056
comment: Phenotype [hp:0002848] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Specific anti-polysaccharide antibody deficiency
in dataset: phenotype

Delayed calcaneal ossification [hp:0008142]
type: SIO_010056
comment: Phenotype [hp:0008142] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed calcaneal ossification
in dataset: phenotype

Spinal stenosis with reduced interpedicular distance [hp:0005733]
type: SIO_010056
comment: Phenotype [hp:0005733] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinal stenosis with reduced interpedicular distance
in dataset: phenotype

Irregular ossification at anterior rib ends [hp:0006598]
type: SIO_010056
comment: Phenotype [hp:0006598] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular ossification at anterior rib ends
in dataset: phenotype

Increased extraneuronal autofluorescent lipopigment [hp:0003463]
type: SIO_010056
comment: Phenotype [hp:0003463] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased extraneuronal autofluorescent lipopigment
in dataset: phenotype

Hyperaldosteronism [hp:0000859]
type: SIO_010056
comment: Phenotype [hp:0000859] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperaldosteronism
in dataset: phenotype

Microtia, third degree [hp:0011267]
type: SIO_010056
comment: Phenotype [hp:0011267] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microtia, third degree
in dataset: phenotype

Rarefaction of retinal pigmentation [hp:0007961]
type: SIO_010056
comment: Phenotype [hp:0007961] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rarefaction of retinal pigmentation
in dataset: phenotype

Asthma [hp:0002099]
type: SIO_010056
comment: Phenotype [hp:0002099] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Asthma
in dataset: phenotype

Ganglioneuroma [hp:0003005]
type: SIO_010056
comment: Phenotype [hp:0003005] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ganglioneuroma
in dataset: phenotype

Atheromatosis [hp:0002635]
type: SIO_010056
comment: Phenotype [hp:0002635] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atheromatosis
in dataset: phenotype

Markedly reduced T cell function [hp:0005409]
type: SIO_010056
comment: Phenotype [hp:0005409] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Markedly reduced T cell function
in dataset: phenotype

Episodic flaccid weakness [hp:0003752]
type: SIO_010056
comment: Phenotype [hp:0003752] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic flaccid weakness
in dataset: phenotype

Midline brain calcifications [hp:0007045]
type: SIO_010056
comment: Phenotype [hp:0007045] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Midline brain calcifications
in dataset: phenotype

Anteriorly placed odontoid process [hp:0004608]
type: SIO_010056
comment: Phenotype [hp:0004608] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anteriorly placed odontoid process
in dataset: phenotype

Subaortic stenosis [hp:0001682]
type: SIO_010056
comment: Phenotype [hp:0001682] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subaortic stenosis
in dataset: phenotype

Uric acid nephrolithiasis [hp:0000791]
type: SIO_010056
comment: Phenotype [hp:0000791] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Uric acid nephrolithiasis
in dataset: phenotype

Abnormality of the preputium [hp:0100587]
type: SIO_010056
comment: Phenotype [hp:0100587] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the preputium
in dataset: phenotype

Steep acetabular roof [hp:0010455]
type: SIO_010056
comment: Phenotype [hp:0010455] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Steep acetabular roof
in dataset: phenotype

Conical tooth [hp:0000698]
type: SIO_010056
comment: Phenotype [hp:0000698] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Conical tooth
in dataset: phenotype

Renovascular hypertension [hp:0100817]
type: SIO_010056
comment: Phenotype [hp:0100817] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renovascular hypertension
in dataset: phenotype

Long fibula [hp:0003085]
type: SIO_010056
comment: Phenotype [hp:0003085] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long fibula
in dataset: phenotype

Absence of lymph node germinal center [hp:0002849]
type: SIO_010056
comment: Phenotype [hp:0002849] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of lymph node germinal center
in dataset: phenotype

Paradoxical increased cortisol secretion on dexamethasone suppression test [hp:0003466]
type: SIO_010056
comment: Phenotype [hp:0003466] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paradoxical increased cortisol secretion on dexamethasone suppression test
in dataset: phenotype

Thickening of the glomerular basement membrane [hp:0004722]
type: SIO_010056
comment: Phenotype [hp:0004722] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thickening of the glomerular basement membrane
in dataset: phenotype

Blindness [hp:0000618]
type: SIO_010056
comment: Phenotype [hp:0000618] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Blindness
in dataset: phenotype

Folate deficiency [hp:0100507]
type: SIO_010056
comment: Phenotype [hp:0100507] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Folate deficiency
in dataset: phenotype

Speckled corneal dystrophy [hp:0007962]
type: SIO_010056
comment: Phenotype [hp:0007962] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Speckled corneal dystrophy
in dataset: phenotype

Diaphragmatic paralysis [hp:0006597]
type: SIO_010056
comment: Phenotype [hp:0006597] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diaphragmatic paralysis
in dataset: phenotype

Absent vertebral body mineralization [hp:0004605]
type: SIO_010056
comment: Phenotype [hp:0004605] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent vertebral body mineralization
in dataset: phenotype

Arteriosclerosis [hp:0002634]
type: SIO_010056
comment: Phenotype [hp:0002634] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arteriosclerosis
in dataset: phenotype

Polar cataract [hp:0010696]
type: SIO_010056
comment: Phenotype [hp:0010696] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polar cataract
in dataset: phenotype

Cerebellar hypoplasia [hp:0001321]
type: SIO_010056
comment: Phenotype [hp:0001321] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebellar hypoplasia
in dataset: phenotype

Cervical cord compression [hp:0002341]
type: SIO_010056
comment: Phenotype [hp:0002341] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cervical cord compression
in dataset: phenotype

Fragile skin [hp:0001030]
type: SIO_010056
comment: Phenotype [hp:0001030] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fragile skin
in dataset: phenotype

Laryngeal stenosis [hp:0001602]
type: SIO_010056
comment: Phenotype [hp:0001602] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laryngeal stenosis
in dataset: phenotype

Ectopia cordis [hp:0001683]
type: SIO_010056
comment: Phenotype [hp:0001683] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopia cordis
in dataset: phenotype

Erythema nodosum [hp:0012219]
type: SIO_010056
comment: Phenotype [hp:0012219] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Erythema nodosum
in dataset: phenotype

Diastema [hp:0000699]
type: SIO_010056
comment: Phenotype [hp:0000699] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diastema
in dataset: phenotype

Mild postnatal growth retardation [hp:0001530]
type: SIO_010056
comment: Phenotype [hp:0001530] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mild postnatal growth retardation
in dataset: phenotype

Vascular tortuosity [hp:0004948]
type: SIO_010056
comment: Phenotype [hp:0004948] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vascular tortuosity
in dataset: phenotype

Cone-shaped epiphyses of the phalanges of the hand [hp:0010230]
type: SIO_010056
comment: Phenotype [hp:0010230] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cone-shaped epiphyses of the phalanges of the hand
in dataset: phenotype

Elevated 8(9)-cholestenol [hp:0003465]
type: SIO_010056
comment: Phenotype [hp:0003465] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated 8(9)-cholestenol
in dataset: phenotype

Long thorax [hp:0100818]
type: SIO_010056
comment: Phenotype [hp:0100818] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long thorax
in dataset: phenotype

Acromesomelia [hp:0003086]
type: SIO_010056
comment: Phenotype [hp:0003086] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acromesomelia
in dataset: phenotype

L-2-hydroxyglutaric acidemia [hp:0040147]
type: SIO_010056
comment: Phenotype [hp:0040147] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: L-2-hydroxyglutaric acidemia
in dataset: phenotype

Aplasia/hypoplasia of the humerus [hp:0006507]
type: SIO_010056
comment: Phenotype [hp:0006507] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/hypoplasia of the humerus
in dataset: phenotype

Macroreticular retinal dystrophy [hp:0007963]
type: SIO_010056
comment: Phenotype [hp:0007963] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macroreticular retinal dystrophy
in dataset: phenotype

Colon cancer [hp:0003003]
type: SIO_010056
comment: Phenotype [hp:0003003] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Colon cancer
in dataset: phenotype

Decreased number of CD4+ T cells [hp:0005407]
type: SIO_010056
comment: Phenotype [hp:0005407] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased number of CD4+ T cells
in dataset: phenotype

Focal white matter lesions [hp:0007042]
type: SIO_010056
comment: Phenotype [hp:0007042] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Focal white matter lesions
in dataset: phenotype

Cortical irregularity [hp:0005731]
type: SIO_010056
comment: Phenotype [hp:0005731] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cortical irregularity
in dataset: phenotype

Postaxial oligodactyly [hp:0006210]
type: SIO_010056
comment: Phenotype [hp:0006210] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Postaxial oligodactyly
in dataset: phenotype

Membranoproliferative glomerulonephritis [hp:0000793]
type: SIO_010056
comment: Phenotype [hp:0000793] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Membranoproliferative glomerulonephritis
in dataset: phenotype

Unossified vertebral bodies [hp:0004606]
type: SIO_010056
comment: Phenotype [hp:0004606] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unossified vertebral bodies
in dataset: phenotype

Asymmetric limb muscle stiffness [hp:0007156]
type: SIO_010056
comment: Phenotype [hp:0007156] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Asymmetric limb muscle stiffness
in dataset: phenotype

Vasculitis [hp:0002633]
type: SIO_010056
comment: Phenotype [hp:0002633] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vasculitis
in dataset: phenotype

Increased muscle fatiguability [hp:0003750]
type: SIO_010056
comment: Phenotype [hp:0003750] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased muscle fatiguability
in dataset: phenotype

Laryngomalacia [hp:0001601]
type: SIO_010056
comment: Phenotype [hp:0001601] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laryngomalacia
in dataset: phenotype

Premature ovarian failure [hp:0008209]
type: SIO_010056
comment: Phenotype [hp:0008209] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature ovarian failure
in dataset: phenotype

Caudate atrophy [hp:0002340]
type: SIO_010056
comment: Phenotype [hp:0002340] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Caudate atrophy
in dataset: phenotype

Cerebellar vermis hypoplasia [hp:0001320]
type: SIO_010056
comment: Phenotype [hp:0001320] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebellar vermis hypoplasia
in dataset: phenotype

Urogenital fistula [hp:0100589]
type: SIO_010056
comment: Phenotype [hp:0100589] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urogenital fistula
in dataset: phenotype

Secundum atrial septal defect [hp:0001684]
type: SIO_010056
comment: Phenotype [hp:0001684] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Secundum atrial septal defect
in dataset: phenotype

Failure to thrive in infancy [hp:0001531]
type: SIO_010056
comment: Phenotype [hp:0001531] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Failure to thrive in infancy
in dataset: phenotype

Alveolar soft part sarcoma [hp:0012218]
type: SIO_010056
comment: Phenotype [hp:0012218] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Alveolar soft part sarcoma
in dataset: phenotype

Abnormality of the aryepiglottic fold [hp:0008744]
type: SIO_010056
comment: Phenotype [hp:0008744] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the aryepiglottic fold
in dataset: phenotype

Paroxysmal drowsiness [hp:0002330]
type: SIO_010056
comment: Phenotype [hp:0002330] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paroxysmal drowsiness
in dataset: phenotype

Crusting erythematous dermatitis [hp:0007473]
type: SIO_010056
comment: Phenotype [hp:0007473] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Crusting erythematous dermatitis
in dataset: phenotype

Bifid distal phalanx of toe [hp:0001853]
type: SIO_010056
comment: Phenotype [hp:0001853] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid distal phalanx of toe
in dataset: phenotype

Abnormality of earlobe [hp:0000363]
type: SIO_010056
comment: Phenotype [hp:0000363] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of earlobe
in dataset: phenotype

Cystic hygroma [hp:0000476]
type: SIO_010056
comment: Phenotype [hp:0000476] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cystic hygroma
in dataset: phenotype

Arteriovenous fistula [hp:0004947]
type: SIO_010056
comment: Phenotype [hp:0004947] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arteriovenous fistula
in dataset: phenotype

Radial deviation of the hand [hp:0009486]
type: SIO_010056
comment: Phenotype [hp:0009486] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Radial deviation of the hand
in dataset: phenotype

Gonadal hypoplasia [hp:0008639]
type: SIO_010056
comment: Phenotype [hp:0008639] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gonadal hypoplasia
in dataset: phenotype

Failure to thrive secondary to recurrent infections [hp:0008866]
type: SIO_010056
comment: Phenotype [hp:0008866] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Failure to thrive secondary to recurrent infections
in dataset: phenotype

Soft, doughy skin [hp:0001027]
type: SIO_010056
comment: Phenotype [hp:0001027] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Soft, doughy skin
in dataset: phenotype

Sutural cataract [hp:0010695]
type: SIO_010056
comment: Phenotype [hp:0010695] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sutural cataract
in dataset: phenotype

Plantar pits [hp:0010612]
type: SIO_010056
comment: Phenotype [hp:0010612] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Plantar pits
in dataset: phenotype

Budd-Chiari syndrome [hp:0002639]
type: SIO_010056
comment: Phenotype [hp:0002639] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Budd-Chiari syndrome
in dataset: phenotype

Elevated serum transaminases during infections [hp:0008150]
type: SIO_010056
comment: Phenotype [hp:0008150] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated serum transaminases during infections
in dataset: phenotype

Hereditary nonpolyposis colorectal carcinoma [hp:0006716]
type: SIO_010056
comment: Phenotype [hp:0006716] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hereditary nonpolyposis colorectal carcinoma
in dataset: phenotype

Urinary hesitancy [hp:0000019]
type: SIO_010056
comment: Phenotype [hp:0000019] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urinary hesitancy
in dataset: phenotype

Multiple renal cysts [hp:0005562]
type: SIO_010056
comment: Phenotype [hp:0005562] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple renal cysts
in dataset: phenotype

Elevated long chain fatty acids [hp:0003455]
type: SIO_010056
comment: Phenotype [hp:0003455] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated long chain fatty acids
in dataset: phenotype

Azotemia [hp:0002157]
type: SIO_010056
comment: Phenotype [hp:0002157] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Azotemia
in dataset: phenotype

Respiratory tract infection [hp:0011947]
type: SIO_010056
comment: Phenotype [hp:0011947] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Respiratory tract infection
in dataset: phenotype

Premature osteoarthritis [hp:0003088]
type: SIO_010056
comment: Phenotype [hp:0003088] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature osteoarthritis
in dataset: phenotype

Atrophy/Degeneration affecting the brainstem [hp:0007366]
type: SIO_010056
comment: Phenotype [hp:0007366] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atrophy/Degeneration affecting the brainstem
in dataset: phenotype

Headache (with pheochromocytoma) [hp:0002331]
type: SIO_010056
comment: Phenotype [hp:0002331] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Headache (with pheochromocytoma)
in dataset: phenotype

Gout (feet) [hp:0001854]
type: SIO_010056
comment: Phenotype [hp:0001854] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gout (feet)
in dataset: phenotype

Optic nerve compression [hp:0007807]
type: SIO_010056
comment: Phenotype [hp:0007807] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Optic nerve compression
in dataset: phenotype

Broad neck [hp:0000475]
type: SIO_010056
comment: Phenotype [hp:0000475] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad neck
in dataset: phenotype

Primary hyperparathyroidism [hp:0008200]
type: SIO_010056
comment: Phenotype [hp:0008200] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Primary hyperparathyroidism
in dataset: phenotype

Hemangioma [hp:0001028]
type: SIO_010056
comment: Phenotype [hp:0001028] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemangioma
in dataset: phenotype

Otosclerosis [hp:0000362]
type: SIO_010056
comment: Phenotype [hp:0000362] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Otosclerosis
in dataset: phenotype

Supernumerary nipple [hp:0002558]
type: SIO_010056
comment: Phenotype [hp:0002558] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Supernumerary nipple
in dataset: phenotype

Pulmonary capillary hemangiomatosis [hp:0005954]
type: SIO_010056
comment: Phenotype [hp:0005954] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary capillary hemangiomatosis
in dataset: phenotype

Frontal hirsutism [hp:0011335]
type: SIO_010056
comment: Phenotype [hp:0011335] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontal hirsutism
in dataset: phenotype

Scapulohumeral synostosis [hp:0006595]
type: SIO_010056
comment: Phenotype [hp:0006595] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scapulohumeral synostosis
in dataset: phenotype

Decreased numbers of nephrons [hp:0005563]
type: SIO_010056
comment: Phenotype [hp:0005563] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased numbers of nephrons
in dataset: phenotype

Low urinary cyclic AMP response to PTH administration [hp:0003456]
type: SIO_010056
comment: Phenotype [hp:0003456] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low urinary cyclic AMP response to PTH administration
in dataset: phenotype

Homocystinuria [hp:0002156]
type: SIO_010056
comment: Phenotype [hp:0002156] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Homocystinuria
in dataset: phenotype

Central adrenal insufficiency [hp:0011734]
type: SIO_010056
comment: Phenotype [hp:0011734] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Central adrenal insufficiency
in dataset: phenotype

Hearing impairment [hp:0000365]
type: SIO_010056
comment: Phenotype [hp:0000365] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hearing impairment
in dataset: phenotype

Inlet ventricular septal defect [hp:0011622]
type: SIO_010056
comment: Phenotype [hp:0011622] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inlet ventricular septal defect
in dataset: phenotype

Abnormality of the eye [hp:0000478]
type: SIO_010056
comment: Phenotype [hp:0000478] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the eye
in dataset: phenotype

Absent glenoid fossa [hp:0006591]
type: SIO_010056
comment: Phenotype [hp:0006591] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent glenoid fossa
in dataset: phenotype

Lack of peer relationships [hp:0002332]
type: SIO_010056
comment: Phenotype [hp:0002332] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lack of peer relationships
in dataset: phenotype

Cystoid macular degeneration [hp:0008028]
type: SIO_010056
comment: Phenotype [hp:0008028] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cystoid macular degeneration
in dataset: phenotype

Hypoplastic nipples [hp:0002557]
type: SIO_010056
comment: Phenotype [hp:0002557] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic nipples
in dataset: phenotype

Poikiloderma [hp:0001029]
type: SIO_010056
comment: Phenotype [hp:0001029] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poikiloderma
in dataset: phenotype

Pulverulent Cataract [hp:0010693]
type: SIO_010056
comment: Phenotype [hp:0010693] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulverulent Cataract
in dataset: phenotype

Aplasia/Hypoplasia of the sternum [hp:0006714]
type: SIO_010056
comment: Phenotype [hp:0006714] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the sternum
in dataset: phenotype

Axial muscle stiffness [hp:0006921]
type: SIO_010056
comment: Phenotype [hp:0006921] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Axial muscle stiffness
in dataset: phenotype

Hemifacial spasm [hp:0010828]
type: SIO_010056
comment: Phenotype [hp:0010828] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemifacial spasm
in dataset: phenotype

Cerebral ischemia [hp:0002637]
type: SIO_010056
comment: Phenotype [hp:0002637] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral ischemia
in dataset: phenotype

Abnormal CNS myelination [hp:0011400]
type: SIO_010056
comment: Phenotype [hp:0011400] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal CNS myelination
in dataset: phenotype

Fibroma [hp:0010614]
type: SIO_010056
comment: Phenotype [hp:0010614] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fibroma
in dataset: phenotype

Heparan sulfate excretion in urine [hp:0002159]
type: SIO_010056
comment: Phenotype [hp:0002159] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Heparan sulfate excretion in urine
in dataset: phenotype

Periarticular subcutaneous nodules [hp:0007470]
type: SIO_010056
comment: Phenotype [hp:0007470] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Periarticular subcutaneous nodules
in dataset: phenotype

Retinal nonattachment [hp:0007899]
type: SIO_010056
comment: Phenotype [hp:0007899] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal nonattachment
in dataset: phenotype

Optic nerve hypoplasia [hp:0000609]
type: SIO_010056
comment: Phenotype [hp:0000609] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Optic nerve hypoplasia
in dataset: phenotype

EMG abnormality [hp:0003457]
type: SIO_010056
comment: Phenotype [hp:0003457] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EMG abnormality
in dataset: phenotype

Interstitial pneumonitis [hp:0006515]
type: SIO_010056
comment: Phenotype [hp:0006515] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Interstitial pneumonitis
in dataset: phenotype

Punctate corneal dystrophy [hp:0007809]
type: SIO_010056
comment: Phenotype [hp:0007809] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Punctate corneal dystrophy
in dataset: phenotype

Hearing abnormality [hp:0000364]
type: SIO_010056
comment: Phenotype [hp:0000364] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hearing abnormality
in dataset: phenotype

Ectopia of the spleen [hp:0010452]
type: SIO_010056
comment: Phenotype [hp:0010452] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopia of the spleen
in dataset: phenotype

Sandal gap [hp:0001852]
type: SIO_010056
comment: Phenotype [hp:0001852] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sandal gap
in dataset: phenotype

Muscular ventricular septal defect [hp:0011623]
type: SIO_010056
comment: Phenotype [hp:0011623] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscular ventricular septal defect
in dataset: phenotype

Coronal hypospadias [hp:0008743]
type: SIO_010056
comment: Phenotype [hp:0008743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coronal hypospadias
in dataset: phenotype

Microglossia [hp:0000171]
type: SIO_010056
comment: Phenotype [hp:0000171] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microglossia
in dataset: phenotype

Metaphyseal cupping of metacarpals [hp:0006028]
type: SIO_010056
comment: Phenotype [hp:0006028] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metaphyseal cupping of metacarpals
in dataset: phenotype

Arnold-Chiari type I malformation [hp:0007099]
type: SIO_010056
comment: Phenotype [hp:0007099] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arnold-Chiari type I malformation
in dataset: phenotype

Motor deterioration [hp:0002333]
type: SIO_010056
comment: Phenotype [hp:0002333] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Motor deterioration
in dataset: phenotype

Asymmetric crying face [hp:0011333]
type: SIO_010056
comment: Phenotype [hp:0011333] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Asymmetric crying face
in dataset: phenotype

Nonprogressive disorder [hp:0003680]
type: SIO_010056
comment: Phenotype [hp:0003680] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonprogressive disorder
in dataset: phenotype

Glomus tympanicum paraganglioma [hp:0006715]
type: SIO_010056
comment: Phenotype [hp:0006715] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glomus tympanicum paraganglioma
in dataset: phenotype

Right aortic arch [hp:0012020]
type: SIO_010056
comment: Phenotype [hp:0012020] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Right aortic arch
in dataset: phenotype

Mild hearing impairment [hp:0012712]
type: SIO_010056
comment: Phenotype [hp:0012712] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mild hearing impairment
in dataset: phenotype

Rib segmentation abnormalities [hp:0006655]
type: SIO_010056
comment: Phenotype [hp:0006655] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rib segmentation abnormalities
in dataset: phenotype

Delayed peripheral myelination [hp:0011401]
type: SIO_010056
comment: Phenotype [hp:0011401] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed peripheral myelination
in dataset: phenotype

Anomalous rib insertion to vertebrae [hp:0006593]
type: SIO_010056
comment: Phenotype [hp:0006593] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anomalous rib insertion to vertebrae
in dataset: phenotype

Periostosis [hp:0030314]
type: SIO_010056
comment: Phenotype [hp:0030314] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Periostosis
in dataset: phenotype

Decreased pulmonary function [hp:0005952]
type: SIO_010056
comment: Phenotype [hp:0005952] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased pulmonary function
in dataset: phenotype

Superficial thrombophlebitis [hp:0002638]
type: SIO_010056
comment: Phenotype [hp:0002638] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Superficial thrombophlebitis
in dataset: phenotype

EMG: myopathic abnormalities [hp:0003458]
type: SIO_010056
comment: Phenotype [hp:0003458] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EMG: myopathic abnormalities
in dataset: phenotype

Impaired temperature sensation [hp:0010829]
type: SIO_010056
comment: Phenotype [hp:0010829] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired temperature sensation
in dataset: phenotype

Abnormality of bone marrow cell morphology [hp:0005561]
type: SIO_010056
comment: Phenotype [hp:0005561] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of bone marrow cell morphology
in dataset: phenotype

Cerebral aneurysm [hp:0004944]
type: SIO_010056
comment: Phenotype [hp:0004944] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral aneurysm
in dataset: phenotype

Intraalveolar nodular calcifications [hp:0006514]
type: SIO_010056
comment: Phenotype [hp:0006514] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intraalveolar nodular calcifications
in dataset: phenotype

Short chordae tendineae of the mitral valve [hp:0011580]
type: SIO_010056
comment: Phenotype [hp:0011580] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short chordae tendineae of the mitral valve
in dataset: phenotype

Pneumonia [hp:0002090]
type: SIO_010056
comment: Phenotype [hp:0002090] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pneumonia
in dataset: phenotype

Renal steatosis [hp:0000799]
type: SIO_010056
comment: Phenotype [hp:0000799] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal steatosis
in dataset: phenotype

Abnormality of the cerebellar vermis [hp:0002334]
type: SIO_010056
comment: Phenotype [hp:0002334] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the cerebellar vermis
in dataset: phenotype

Lymphadenitis [hp:0002840]
type: SIO_010056
comment: Phenotype [hp:0002840] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lymphadenitis
in dataset: phenotype

Oligodactyly (hands) [hp:0001180]
type: SIO_010056
comment: Phenotype [hp:0001180] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oligodactyly (hands)
in dataset: phenotype

Longitudinal vaginal septum [hp:0008740]
type: SIO_010056
comment: Phenotype [hp:0008740] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Longitudinal vaginal septum
in dataset: phenotype

Bladder diverticulum [hp:0000015]
type: SIO_010056
comment: Phenotype [hp:0000015] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bladder diverticulum
in dataset: phenotype

Abnormal dermatoglyphics [hp:0007477]
type: SIO_010056
comment: Phenotype [hp:0007477] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal dermatoglyphics
in dataset: phenotype

Corneal opacity [hp:0007957]
type: SIO_010056
comment: Phenotype [hp:0007957] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corneal opacity
in dataset: phenotype

Accelerated atherosclerosis [hp:0004943]
type: SIO_010056
comment: Phenotype [hp:0004943] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Accelerated atherosclerosis
in dataset: phenotype

Umbilical hernia [hp:0001537]
type: SIO_010056
comment: Phenotype [hp:0001537] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Umbilical hernia
in dataset: phenotype

Polyclonal elevation of IgM [hp:0003459]
type: SIO_010056
comment: Phenotype [hp:0003459] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polyclonal elevation of IgM
in dataset: phenotype

Short distal phalanx of toe [hp:0001857]
type: SIO_010056
comment: Phenotype [hp:0001857] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short distal phalanx of toe
in dataset: phenotype

Demyelinating sensory neuropathy [hp:0011402]
type: SIO_010056
comment: Phenotype [hp:0011402] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Demyelinating sensory neuropathy
in dataset: phenotype

Accelerated skeletal maturation [hp:0005616]
type: SIO_010056
comment: Phenotype [hp:0005616] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Accelerated skeletal maturation
in dataset: phenotype

Cartilaginous trachea [hp:0005347]
type: SIO_010056
comment: Phenotype [hp:0005347] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cartilaginous trachea
in dataset: phenotype

Hyperkalemia [hp:0002153]
type: SIO_010056
comment: Phenotype [hp:0002153] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperkalemia
in dataset: phenotype

Hemifacial hypoplasia [hp:0011332]
type: SIO_010056
comment: Phenotype [hp:0011332] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemifacial hypoplasia
in dataset: phenotype

Absent rod-and cone-mediated responses on ERG [hp:0007688]
type: SIO_010056
comment: Phenotype [hp:0007688] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent rod-and cone-mediated responses on ERG
in dataset: phenotype

Restrictive lung disease [hp:0002091]
type: SIO_010056
comment: Phenotype [hp:0002091] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Restrictive lung disease
in dataset: phenotype

Agenesis of cerebellar vermis [hp:0002335]
type: SIO_010056
comment: Phenotype [hp:0002335] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Agenesis of cerebellar vermis
in dataset: phenotype

Precocious puberty with Sertoli cell tumor [hp:0008204]
type: SIO_010056
comment: Phenotype [hp:0008204] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Precocious puberty with Sertoli cell tumor
in dataset: phenotype

Skin dimple over apex of long bone angulation [hp:0001024]
type: SIO_010056
comment: Phenotype [hp:0001024] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skin dimple over apex of long bone angulation
in dataset: phenotype

Oligospermia [hp:0000798]
type: SIO_010056
comment: Phenotype [hp:0000798] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oligospermia
in dataset: phenotype

Postnatal macrocephaly [hp:0005490]
type: SIO_010056
comment: Phenotype [hp:0005490] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Postnatal macrocephaly
in dataset: phenotype

Adducted thumb [hp:0001181]
type: SIO_010056
comment: Phenotype [hp:0001181] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adducted thumb
in dataset: phenotype

Enlarged epiphysis of the proximal phalanx of the 2nd finger [hp:0009527]
type: SIO_010056
comment: Phenotype [hp:0009527] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged epiphysis of the proximal phalanx of the 2nd finger
in dataset: phenotype

Small epiphyses of the phalanges of the hand [hp:0010236]
type: SIO_010056
comment: Phenotype [hp:0010236] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small epiphyses of the phalanges of the hand
in dataset: phenotype

Recurrent bronchiolitis [hp:0100501]
type: SIO_010056
comment: Phenotype [hp:0100501] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent bronchiolitis
in dataset: phenotype

Urinary retention [hp:0000016]
type: SIO_010056
comment: Phenotype [hp:0000016] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urinary retention
in dataset: phenotype

Abnormality of the pons [hp:0007361]
type: SIO_010056
comment: Phenotype [hp:0007361] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the pons
in dataset: phenotype

Lobar holoprosencephaly [hp:0006870]
type: SIO_010056
comment: Phenotype [hp:0006870] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lobar holoprosencephaly
in dataset: phenotype

Laryngeal web [hp:0005950]
type: SIO_010056
comment: Phenotype [hp:0005950] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laryngeal web
in dataset: phenotype

Aortic aneurysm [hp:0004942]
type: SIO_010056
comment: Phenotype [hp:0004942] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aortic aneurysm
in dataset: phenotype

Abnormal facial expression [hp:0005346]
type: SIO_010056
comment: Phenotype [hp:0005346] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal facial expression
in dataset: phenotype

Hypoplasia of first ribs [hp:0006657]
type: SIO_010056
comment: Phenotype [hp:0006657] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of first ribs
in dataset: phenotype

Unilateral ptosis [hp:0007687]
type: SIO_010056
comment: Phenotype [hp:0007687] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral ptosis
in dataset: phenotype

Posterior synechiae of the anterior chamber [hp:0011484]
type: SIO_010056
comment: Phenotype [hp:0011484] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior synechiae of the anterior chamber
in dataset: phenotype

Urticaria [hp:0001025]
type: SIO_010056
comment: Phenotype [hp:0001025] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urticaria
in dataset: phenotype

Palmar pits [hp:0010610]
type: SIO_010056
comment: Phenotype [hp:0010610] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palmar pits
in dataset: phenotype

Pulmonary hypertension [hp:0002092]
type: SIO_010056
comment: Phenotype [hp:0002092] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary hypertension
in dataset: phenotype

Calcification of cartilage [hp:0100593]
type: SIO_010056
comment: Phenotype [hp:0100593] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcification of cartilage
in dataset: phenotype

Nonepidermolytic palmoplantar keratoderma [hp:0007404]
type: SIO_010056
comment: Phenotype [hp:0007404] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nonepidermolytic palmoplantar keratoderma
in dataset: phenotype

Abnormality of the palate [hp:0000174]
type: SIO_010056
comment: Phenotype [hp:0000174] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the palate
in dataset: phenotype

Pulsatile tinnitus (tympanic paraganglioma) [hp:0000361]
type: SIO_010056
comment: Phenotype [hp:0000361] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulsatile tinnitus (tympanic paraganglioma)
in dataset: phenotype

Nocturia [hp:0000017]
type: SIO_010056
comment: Phenotype [hp:0000017] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nocturia
in dataset: phenotype

Cerebellar hemorrhage [hp:0011695]
type: SIO_010056
comment: Phenotype [hp:0011695] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebellar hemorrhage
in dataset: phenotype

Recurrent Burkholderia cepacia infections [hp:0002842]
type: SIO_010056
comment: Phenotype [hp:0002842] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent Burkholderia cepacia infections
in dataset: phenotype

Velopharyngeal insufficiency [hp:0000220]
type: SIO_010056
comment: Phenotype [hp:0000220] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Velopharyngeal insufficiency
in dataset: phenotype

Congenital bullous ichthyosiform erythroderma [hp:0007475]
type: SIO_010056
comment: Phenotype [hp:0007475] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital bullous ichthyosiform erythroderma
in dataset: phenotype

Tapered finger [hp:0001182]
type: SIO_010056
comment: Phenotype [hp:0001182] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tapered finger
in dataset: phenotype

Omphalocele [hp:0001539]
type: SIO_010056
comment: Phenotype [hp:0001539] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Omphalocele
in dataset: phenotype

Aplasia of the middle phalanx of the hand [hp:0010239]
type: SIO_010056
comment: Phenotype [hp:0010239] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the middle phalanx of the hand
in dataset: phenotype

Stippled calcification in carpal bones [hp:0004241]
type: SIO_010056
comment: Phenotype [hp:0004241] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stippled calcification in carpal bones
in dataset: phenotype

Laryngeal stridor [hp:0006511]
type: SIO_010056
comment: Phenotype [hp:0006511] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laryngeal stridor
in dataset: phenotype

Metopic synostosis [hp:0011330]
type: SIO_010056
comment: Phenotype [hp:0011330] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metopic synostosis
in dataset: phenotype

Abnormal pupillary function [hp:0007686]
type: SIO_010056
comment: Phenotype [hp:0007686] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal pupillary function
in dataset: phenotype

Respiratory insufficiency [hp:0002093]
type: SIO_010056
comment: Phenotype [hp:0002093] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Respiratory insufficiency
in dataset: phenotype

Hypertriglyceridemia [hp:0002155]
type: SIO_010056
comment: Phenotype [hp:0002155] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertriglyceridemia
in dataset: phenotype

Beaking of vertebral bodies [hp:0004568]
type: SIO_010056
comment: Phenotype [hp:0004568] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Beaking of vertebral bodies
in dataset: phenotype

Large beaked nose [hp:0003683]
type: SIO_010056
comment: Phenotype [hp:0003683] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large beaked nose
in dataset: phenotype

Hypoplasia of the epiglottis [hp:0005349]
type: SIO_010056
comment: Phenotype [hp:0005349] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the epiglottis
in dataset: phenotype

Craniopharyngioma [hp:0030062]
type: SIO_010056
comment: Phenotype [hp:0030062] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Craniopharyngioma
in dataset: phenotype

Childhood onset short-limb short stature [hp:0011405]
type: SIO_010056
comment: Phenotype [hp:0011405] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Childhood onset short-limb short stature
in dataset: phenotype

Intellectual disability [hp:0001249]
type: SIO_010056
comment: Phenotype [hp:0001249] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intellectual disability
in dataset: phenotype

Prolactin deficiency [hp:0008202]
type: SIO_010056
comment: Phenotype [hp:0008202] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolactin deficiency
in dataset: phenotype

Ulnar deviation of the hand [hp:0009487]
type: SIO_010056
comment: Phenotype [hp:0009487] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ulnar deviation of the hand
in dataset: phenotype

Cleft palate [hp:0000175]
type: SIO_010056
comment: Phenotype [hp:0000175] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cleft palate
in dataset: phenotype

Hypertrophy of skin of soles [hp:0007403]
type: SIO_010056
comment: Phenotype [hp:0007403] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertrophy of skin of soles
in dataset: phenotype

Tinnitus [hp:0000360]
type: SIO_010056
comment: Phenotype [hp:0000360] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tinnitus
in dataset: phenotype

Anhidrotic ectodermal dysplasia [hp:0007476]
type: SIO_010056
comment: Phenotype [hp:0007476] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anhidrotic ectodermal dysplasia
in dataset: phenotype

Recurrent fungal infections [hp:0002841]
type: SIO_010056
comment: Phenotype [hp:0002841] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent fungal infections
in dataset: phenotype

Generalized arterial calcification [hp:0004940]
type: SIO_010056
comment: Phenotype [hp:0004940] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized arterial calcification
in dataset: phenotype

Protuberant abdomen [hp:0001538]
type: SIO_010056
comment: Phenotype [hp:0001538] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Protuberant abdomen
in dataset: phenotype

Optic atrophy from cranial nerve compression [hp:0007958]
type: SIO_010056
comment: Phenotype [hp:0007958] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Optic atrophy from cranial nerve compression
in dataset: phenotype

Dyspnea [hp:0002094]
type: SIO_010056
comment: Phenotype [hp:0002094] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dyspnea
in dataset: phenotype

Internally rotated shoulders [hp:0006659]
type: SIO_010056
comment: Phenotype [hp:0006659] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Internally rotated shoulders
in dataset: phenotype

Aplasia/hypoplasia of the femur [hp:0005613]
type: SIO_010056
comment: Phenotype [hp:0005613] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/hypoplasia of the femur
in dataset: phenotype

Peripheral retinal avascularization [hp:0007685]
type: SIO_010056
comment: Phenotype [hp:0007685] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral retinal avascularization
in dataset: phenotype

Chronic obstructive pulmonary disease [hp:0006510]
type: SIO_010056
comment: Phenotype [hp:0006510] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic obstructive pulmonary disease
in dataset: phenotype

Inspiratory stridor [hp:0005348]
type: SIO_010056
comment: Phenotype [hp:0005348] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inspiratory stridor
in dataset: phenotype

Hyperglycinemia [hp:0002154]
type: SIO_010056
comment: Phenotype [hp:0002154] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperglycinemia
in dataset: phenotype

Restrictive heart failure [hp:0005130]
type: SIO_010056
comment: Phenotype [hp:0005130] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Restrictive heart failure
in dataset: phenotype

Low plasma citrulline [hp:0003572]
type: SIO_010056
comment: Phenotype [hp:0003572] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low plasma citrulline
in dataset: phenotype

Erythroid hyperplasia [hp:0012132]
type: SIO_010056
comment: Phenotype [hp:0012132] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Erythroid hyperplasia
in dataset: phenotype

Chronic active hepatitis [hp:0200120]
type: SIO_010056
comment: Phenotype [hp:0200120] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic active hepatitis
in dataset: phenotype

Irregular femoral epiphysis [hp:0006361]
type: SIO_010056
comment: Phenotype [hp:0006361] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular femoral epiphysis
in dataset: phenotype

Progressive retinal degeneration [hp:0007893]
type: SIO_010056
comment: Phenotype [hp:0007893] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive retinal degeneration
in dataset: phenotype

Symmetrical progressive peripheral demyelination [hp:0006873]
type: SIO_010056
comment: Phenotype [hp:0006873] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Symmetrical progressive peripheral demyelination
in dataset: phenotype

Absent nasal bridge [hp:0005285]
type: SIO_010056
comment: Phenotype [hp:0005285] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent nasal bridge
in dataset: phenotype

Polysplenia [hp:0001748]
type: SIO_010056
comment: Phenotype [hp:0001748] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polysplenia
in dataset: phenotype

Gangrene [hp:0100758]
type: SIO_010056
comment: Phenotype [hp:0100758] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gangrene
in dataset: phenotype

Increased axial globe length [hp:0007800]
type: SIO_010056
comment: Phenotype [hp:0007800] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased axial globe length
in dataset: phenotype

Hypoplasia of the bladder [hp:0005343]
type: SIO_010056
comment: Phenotype [hp:0005343] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the bladder
in dataset: phenotype

Neurogenic bladder [hp:0000011]
type: SIO_010056
comment: Phenotype [hp:0000011] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neurogenic bladder
in dataset: phenotype

Gingival hyperkeratosis [hp:0000222]
type: SIO_010056
comment: Phenotype [hp:0000222] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gingival hyperkeratosis
in dataset: phenotype

Absent radius [hp:0003974]
type: SIO_010056
comment: Phenotype [hp:0003974] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent radius
in dataset: phenotype

Infancy onset short-trunk short stature [hp:0011406]
type: SIO_010056
comment: Phenotype [hp:0011406] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Infancy onset short-trunk short stature
in dataset: phenotype

Short tubular bones (hand) [hp:0001248]
type: SIO_010056
comment: Phenotype [hp:0001248] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short tubular bones (hand)
in dataset: phenotype

Increased total bilirubin [hp:0003573]
type: SIO_010056
comment: Phenotype [hp:0003573] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased total bilirubin
in dataset: phenotype

Abnormality of corneal endothelium [hp:0011488]
type: SIO_010056
comment: Phenotype [hp:0011488] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of corneal endothelium
in dataset: phenotype

Hypopigmentation of the fundus [hp:0007894]
type: SIO_010056
comment: Phenotype [hp:0007894] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypopigmentation of the fundus
in dataset: phenotype

Abnormality of ulnar metaphysis [hp:0004039]
type: SIO_010056
comment: Phenotype [hp:0004039] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of ulnar metaphysis
in dataset: phenotype

Progressive cone degeneration [hp:0008020]
type: SIO_010056
comment: Phenotype [hp:0008020] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive cone degeneration
in dataset: phenotype

Clubbing of fingers [hp:0100759]
type: SIO_010056
comment: Phenotype [hp:0100759] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Clubbing of fingers
in dataset: phenotype

Urinary urgency [hp:0000012]
type: SIO_010056
comment: Phenotype [hp:0000012] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urinary urgency
in dataset: phenotype

Maternal hyperphenylalaninemia [hp:0100610]
type: SIO_010056
comment: Phenotype [hp:0100610] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Maternal hyperphenylalaninemia
in dataset: phenotype

Scapulohumeral muscular dystrophy [hp:0008970]
type: SIO_010056
comment: Phenotype [hp:0008970] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scapulohumeral muscular dystrophy
in dataset: phenotype

Numerous pigmented freckles [hp:0007587]
type: SIO_010056
comment: Phenotype [hp:0007587] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Numerous pigmented freckles
in dataset: phenotype

Absent facial hair [hp:0002550]
type: SIO_010056
comment: Phenotype [hp:0002550] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent facial hair
in dataset: phenotype

Noninflammatory macular atrophy [hp:0007401]
type: SIO_010056
comment: Phenotype [hp:0007401] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Noninflammatory macular atrophy
in dataset: phenotype

Furrowed tongue [hp:0000221]
type: SIO_010056
comment: Phenotype [hp:0000221] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Furrowed tongue
in dataset: phenotype

Freckling [hp:0001480]
type: SIO_010056
comment: Phenotype [hp:0001480] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Freckling
in dataset: phenotype

Edema of the dorsum of hands [hp:0007514]
type: SIO_010056
comment: Phenotype [hp:0007514] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Edema of the dorsum of hands
in dataset: phenotype

Abnormality of hair pigmentation [hp:0009887]
type: SIO_010056
comment: Phenotype [hp:0009887] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of hair pigmentation
in dataset: phenotype

Thoracolumbar kyphosis [hp:0005619]
type: SIO_010056
comment: Phenotype [hp:0005619] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thoracolumbar kyphosis
in dataset: phenotype

Atypical or prolonged hepatitis [hp:0200122]
type: SIO_010056
comment: Phenotype [hp:0200122] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atypical or prolonged hepatitis
in dataset: phenotype

Exostosis of the external auditory canal [hp:0004459]
type: SIO_010056
comment: Phenotype [hp:0004459] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exostosis of the external auditory canal
in dataset: phenotype

Hyperglycinuria [hp:0003108]
type: SIO_010056
comment: Phenotype [hp:0003108] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperglycinuria
in dataset: phenotype

Hyperthreoninuria [hp:0003296]
type: SIO_010056
comment: Phenotype [hp:0003296] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperthreoninuria
in dataset: phenotype

Increased serum lactate [hp:0002151]
type: SIO_010056
comment: Phenotype [hp:0002151] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased serum lactate
in dataset: phenotype

Increased corneal thickness [hp:0011487]
type: SIO_010056
comment: Phenotype [hp:0011487] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased corneal thickness
in dataset: phenotype

Abnormal sperm morphology [hp:0012864]
type: SIO_010056
comment: Phenotype [hp:0012864] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal sperm morphology
in dataset: phenotype

Positive regitine blocking test [hp:0003574]
type: SIO_010056
comment: Phenotype [hp:0003574] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Positive regitine blocking test
in dataset: phenotype

Pulmonary lymphangiomyomatosis [hp:0012798]
type: SIO_010056
comment: Phenotype [hp:0012798] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary lymphangiomyomatosis
in dataset: phenotype

Asplenia [hp:0001746]
type: SIO_010056
comment: Phenotype [hp:0001746] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Asplenia
in dataset: phenotype

Granular corneal dystrophy [hp:0007802]
type: SIO_010056
comment: Phenotype [hp:0007802] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Granular corneal dystrophy
in dataset: phenotype

Aplasia/Hypoplasia of the cerebellum [hp:0007360]
type: SIO_010056
comment: Phenotype [hp:0007360] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the cerebellum
in dataset: phenotype

Irregular hyperpigmentation [hp:0007400]
type: SIO_010056
comment: Phenotype [hp:0007400] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular hyperpigmentation
in dataset: phenotype

Decreased taste sensation [hp:0000224]
type: SIO_010056
comment: Phenotype [hp:0000224] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased taste sensation
in dataset: phenotype

Hypoplasia of the uterus [hp:0000013]
type: SIO_010056
comment: Phenotype [hp:0000013] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the uterus
in dataset: phenotype

Abnormal pyramidal signs [hp:0007256]
type: SIO_010056
comment: Phenotype [hp:0007256] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal pyramidal signs
in dataset: phenotype

Nuclear cataract [hp:0100018]
type: SIO_010056
comment: Phenotype [hp:0100018] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nuclear cataract
in dataset: phenotype

Hypoglycemic encephalopathy [hp:0006929]
type: SIO_010056
comment: Phenotype [hp:0006929] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoglycemic encephalopathy
in dataset: phenotype

Triangular epiphysis of the middle phalanx of the 3rd finger [hp:0009331]
type: SIO_010056
comment: Phenotype [hp:0009331] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular epiphysis of the middle phalanx of the 3rd finger
in dataset: phenotype

Short neck [hp:0000470]
type: SIO_010056
comment: Phenotype [hp:0000470] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short neck
in dataset: phenotype

Generalized hypopigmentation [hp:0007513]
type: SIO_010056
comment: Phenotype [hp:0007513] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized hypopigmentation
in dataset: phenotype

Hypoplasia of the lacrimal puncta [hp:0007892]
type: SIO_010056
comment: Phenotype [hp:0007892] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the lacrimal puncta
in dataset: phenotype

Hypercalciuria [hp:0002150]
type: SIO_010056
comment: Phenotype [hp:0002150] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypercalciuria
in dataset: phenotype

Hyperphosphaturia [hp:0003109]
type: SIO_010056
comment: Phenotype [hp:0003109] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperphosphaturia
in dataset: phenotype

Xanthinuria [hp:0010934]
type: SIO_010056
comment: Phenotype [hp:0010934] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Xanthinuria
in dataset: phenotype

Bilateral camptodactyly [hp:0005617]
type: SIO_010056
comment: Phenotype [hp:0005617] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral camptodactyly
in dataset: phenotype

Exaggerated cupid's bow [hp:0002263]
type: SIO_010056
comment: Phenotype [hp:0002263] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exaggerated cupid's bow
in dataset: phenotype

Impaired FSH and LH secretion [hp:0003295]
type: SIO_010056
comment: Phenotype [hp:0003295] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired FSH and LH secretion
in dataset: phenotype

Accessory spleen [hp:0001747]
type: SIO_010056
comment: Phenotype [hp:0001747] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Accessory spleen
in dataset: phenotype

Abnormality of the nares [hp:0005288]
type: SIO_010056
comment: Phenotype [hp:0005288] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the nares
in dataset: phenotype

Increased intracellular sodium [hp:0003575]
type: SIO_010056
comment: Phenotype [hp:0003575] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased intracellular sodium
in dataset: phenotype

Erythroid hypoplasia [hp:0012133]
type: SIO_010056
comment: Phenotype [hp:0012133] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Erythroid hypoplasia
in dataset: phenotype

Abnormality of the carotid arteries [hp:0005344]
type: SIO_010056
comment: Phenotype [hp:0005344] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the carotid arteries
in dataset: phenotype

Cerebral hypoplasia [hp:0006872]
type: SIO_010056
comment: Phenotype [hp:0006872] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral hypoplasia
in dataset: phenotype

Hyperextensibility of the finger joints [hp:0001187]
type: SIO_010056
comment: Phenotype [hp:0001187] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperextensibility of the finger joints
in dataset: phenotype

Pyropoikilocytosis [hp:0004839]
type: SIO_010056
comment: Phenotype [hp:0004839] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pyropoikilocytosis
in dataset: phenotype

Skin fragility with non-scarring blistering [hp:0007585]
type: SIO_010056
comment: Phenotype [hp:0007585] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skin fragility with non-scarring blistering
in dataset: phenotype

Subcutaneous nodule [hp:0001482]
type: SIO_010056
comment: Phenotype [hp:0001482] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subcutaneous nodule
in dataset: phenotype

Spinal cord posterior columns myelin loss [hp:0008311]
type: SIO_010056
comment: Phenotype [hp:0008311] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinal cord posterior columns myelin loss
in dataset: phenotype

Small thenar eminence [hp:0001245]
type: SIO_010056
comment: Phenotype [hp:0001245] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small thenar eminence
in dataset: phenotype

Congenital talipes calcaneovalgus [hp:0005850]
type: SIO_010056
comment: Phenotype [hp:0005850] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital talipes calcaneovalgus
in dataset: phenotype

Chronic hepatitis due to cryptospridium infection [hp:0200124]
type: SIO_010056
comment: Phenotype [hp:0200124] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic hepatitis due to cryptospridium infection
in dataset: phenotype

Thickening of the lateral border of the scapula [hp:0006650]
type: SIO_010056
comment: Phenotype [hp:0006650] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thickening of the lateral border of the scapula
in dataset: phenotype

Sclerodactyly [hp:0011838]
type: SIO_010056
comment: Phenotype [hp:0011838] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sclerodactyly
in dataset: phenotype

Focal clonic seizures [hp:0002266]
type: SIO_010056
comment: Phenotype [hp:0002266] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Focal clonic seizures
in dataset: phenotype

Abnormality of the upper urinary tract [hp:0010935]
type: SIO_010056
comment: Phenotype [hp:0010935] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the upper urinary tract
in dataset: phenotype

Increased cup-to-disc ratio [hp:0012796]
type: SIO_010056
comment: Phenotype [hp:0012796] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased cup-to-disc ratio
in dataset: phenotype

Spina bifida occulta [hp:0003298]
type: SIO_010056
comment: Phenotype [hp:0003298] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spina bifida occulta
in dataset: phenotype

Subperiosteal erosions due to secondary hyperparathyroidism [hp:0003106]
type: SIO_010056
comment: Phenotype [hp:0003106] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subperiosteal erosions due to secondary hyperparathyroidism
in dataset: phenotype

Hand clenching [hp:0001188]
type: SIO_010056
comment: Phenotype [hp:0001188] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hand clenching
in dataset: phenotype

Tenesmus [hp:0012702]
type: SIO_010056
comment: Phenotype [hp:0012702] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tenesmus
in dataset: phenotype

Absent pubic hair [hp:0002555]
type: SIO_010056
comment: Phenotype [hp:0002555] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent pubic hair
in dataset: phenotype

Impaired gluconeogenesis [hp:0005959]
type: SIO_010056
comment: Phenotype [hp:0005959] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired gluconeogenesis
in dataset: phenotype

Shoulder dislocation [hp:0003834]
type: SIO_010056
comment: Phenotype [hp:0003834] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shoulder dislocation
in dataset: phenotype

Long neck [hp:0000472]
type: SIO_010056
comment: Phenotype [hp:0000472] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long neck
in dataset: phenotype

Lack of subcutaneous fatty tissue [hp:0007519]
type: SIO_010056
comment: Phenotype [hp:0007519] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lack of subcutaneous fatty tissue
in dataset: phenotype

Hyperkinesis [hp:0002487]
type: SIO_010056
comment: Phenotype [hp:0002487] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperkinesis
in dataset: phenotype

Unilateral polymicrogyria [hp:0006927]
type: SIO_010056
comment: Phenotype [hp:0006927] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral polymicrogyria
in dataset: phenotype

Punctate vertebral calcifications [hp:0008420]
type: SIO_010056
comment: Phenotype [hp:0008420] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Punctate vertebral calcifications
in dataset: phenotype

Horizontal opticokinetic nystagmus [hp:0008026]
type: SIO_010056
comment: Phenotype [hp:0008026] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Horizontal opticokinetic nystagmus
in dataset: phenotype

Abnormality of the mesentery [hp:0100016]
type: SIO_010056
comment: Phenotype [hp:0100016] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the mesentery
in dataset: phenotype

Abnormal hair whorl [hp:0010721]
type: SIO_010056
comment: Phenotype [hp:0010721] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal hair whorl
in dataset: phenotype

Splenomegaly [hp:0001744]
type: SIO_010056
comment: Phenotype [hp:0001744] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Splenomegaly
in dataset: phenotype

Severe demyelination of the white matter [hp:0007258]
type: SIO_010056
comment: Phenotype [hp:0007258] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe demyelination of the white matter
in dataset: phenotype

Depressed nasal bridge [hp:0005280]
type: SIO_010056
comment: Phenotype [hp:0005280] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Depressed nasal bridge
in dataset: phenotype

Difficulty running [hp:0009046]
type: SIO_010056
comment: Phenotype [hp:0009046] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Difficulty running
in dataset: phenotype

Mitochondrial respiratory chain defects [hp:0200125]
type: SIO_010056
comment: Phenotype [hp:0200125] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mitochondrial respiratory chain defects
in dataset: phenotype

Monochromacy [hp:0007803]
type: SIO_010056
comment: Phenotype [hp:0007803] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Monochromacy
in dataset: phenotype

Short nose [hp:0003196]
type: SIO_010056
comment: Phenotype [hp:0003196] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short nose
in dataset: phenotype

Impaired lymphocyte transformation with phytohemagglutinin [hp:0003347]
type: SIO_010056
comment: Phenotype [hp:0003347] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired lymphocyte transformation with phytohemagglutinin
in dataset: phenotype

Abnormality of cells of the granulocytic lineage [hp:0012135]
type: SIO_010056
comment: Phenotype [hp:0012135] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of cells of the granulocytic lineage
in dataset: phenotype

Exudative retinopathy [hp:0007898]
type: SIO_010056
comment: Phenotype [hp:0007898] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exudative retinopathy
in dataset: phenotype

Large fleshy ears [hp:0002265]
type: SIO_010056
comment: Phenotype [hp:0002265] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large fleshy ears
in dataset: phenotype

Asymmetry of the ears [hp:0010722]
type: SIO_010056
comment: Phenotype [hp:0010722] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Asymmetry of the ears
in dataset: phenotype

Hyperlysinuria [hp:0003297]
type: SIO_010056
comment: Phenotype [hp:0003297] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperlysinuria
in dataset: phenotype

Abnormality of cholesterol metabolism [hp:0003107]
type: SIO_010056
comment: Phenotype [hp:0003107] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of cholesterol metabolism
in dataset: phenotype

Abnormality of the optic disc [hp:0012795]
type: SIO_010056
comment: Phenotype [hp:0012795] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the optic disc
in dataset: phenotype

Renal magnesium wasting [hp:0005567]
type: SIO_010056
comment: Phenotype [hp:0005567] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal magnesium wasting
in dataset: phenotype

Gastrointestinal angiodysplasia [hp:0000471]
type: SIO_010056
comment: Phenotype [hp:0000471] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gastrointestinal angiodysplasia
in dataset: phenotype

Stahl ear [hp:0100015]
type: SIO_010056
comment: Phenotype [hp:0100015] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stahl ear
in dataset: phenotype

Laryngeal hypoplasia [hp:0008749]
type: SIO_010056
comment: Phenotype [hp:0008749] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laryngeal hypoplasia
in dataset: phenotype

Acute leukemia [hp:0002488]
type: SIO_010056
comment: Phenotype [hp:0002488] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute leukemia
in dataset: phenotype

Telangiectasia macularis eruptiva perstans [hp:0007583]
type: SIO_010056
comment: Phenotype [hp:0007583] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Telangiectasia macularis eruptiva perstans
in dataset: phenotype

Gingival bleeding [hp:0000225]
type: SIO_010056
comment: Phenotype [hp:0000225] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gingival bleeding
in dataset: phenotype

Exercise-induced rhabdomyolysis [hp:0009045]
type: SIO_010056
comment: Phenotype [hp:0009045] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exercise-induced rhabdomyolysis
in dataset: phenotype

Hypoplastic nasal bridge [hp:0005281]
type: SIO_010056
comment: Phenotype [hp:0005281] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic nasal bridge
in dataset: phenotype

Abnormality of the nose [hp:0000366]
type: SIO_010056
comment: Phenotype [hp:0000366] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the nose
in dataset: phenotype

Unossified sacrum [hp:0030290]
type: SIO_010056
comment: Phenotype [hp:0030290] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unossified sacrum
in dataset: phenotype

Decreased muscle mass [hp:0003199]
type: SIO_010056
comment: Phenotype [hp:0003199] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased muscle mass
in dataset: phenotype

Uncontrolled eye movements [hp:0007738]
type: SIO_010056
comment: Phenotype [hp:0007738] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Uncontrolled eye movements
in dataset: phenotype

Paroxysmal dystonia [hp:0002268]
type: SIO_010056
comment: Phenotype [hp:0002268] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paroxysmal dystonia
in dataset: phenotype

Hyperalaninemia [hp:0003348]
type: SIO_010056
comment: Phenotype [hp:0003348] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperalaninemia
in dataset: phenotype

Autonomic bladder dysfunction [hp:0005341]
type: SIO_010056
comment: Phenotype [hp:0005341] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autonomic bladder dysfunction
in dataset: phenotype

Absence of renal corticomedullary differentiation [hp:0005564]
type: SIO_010056
comment: Phenotype [hp:0005564] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of renal corticomedullary differentiation
in dataset: phenotype

Conjugated hyperbilirubinemia [hp:0002908]
type: SIO_010056
comment: Phenotype [hp:0002908] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Conjugated hyperbilirubinemia
in dataset: phenotype

Breathing dysregulation [hp:0005957]
type: SIO_010056
comment: Phenotype [hp:0005957] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Breathing dysregulation
in dataset: phenotype

Molybdenum cofactor deficiency [hp:0003570]
type: SIO_010056
comment: Phenotype [hp:0003570] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Molybdenum cofactor deficiency
in dataset: phenotype

Cerebral arteriovenous malformation [hp:0002408]
type: SIO_010056
comment: Phenotype [hp:0002408] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral arteriovenous malformation
in dataset: phenotype

Cystic lesions of the pinnae [hp:0010723]
type: SIO_010056
comment: Phenotype [hp:0010723] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cystic lesions of the pinnae
in dataset: phenotype

Cerebellar agenesis [hp:0012642]
type: SIO_010056
comment: Phenotype [hp:0012642] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebellar agenesis
in dataset: phenotype

Short thumb [hp:0009778]
type: SIO_010056
comment: Phenotype [hp:0009778] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short thumb
in dataset: phenotype

Palmoplantar cutis laxa [hp:0007517]
type: SIO_010056
comment: Phenotype [hp:0007517] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palmoplantar cutis laxa
in dataset: phenotype

Vertebral wedging [hp:0008422]
type: SIO_010056
comment: Phenotype [hp:0008422] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vertebral wedging
in dataset: phenotype

Highly arched eyebrow [hp:0002553]
type: SIO_010056
comment: Phenotype [hp:0002553] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Highly arched eyebrow
in dataset: phenotype

Congenital nuclear cataract [hp:0008024]
type: SIO_010056
comment: Phenotype [hp:0008024] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital nuclear cataract
in dataset: phenotype

Epiretinal membrane [hp:0100014]
type: SIO_010056
comment: Phenotype [hp:0100014] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Epiretinal membrane
in dataset: phenotype

Thickened nuchal skin fold [hp:0000474]
type: SIO_010056
comment: Phenotype [hp:0000474] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thickened nuchal skin fold
in dataset: phenotype

Low-set ears [hp:0000369]
type: SIO_010056
comment: Phenotype [hp:0000369] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low-set ears
in dataset: phenotype

Nasal obstruction [hp:0001742]
type: SIO_010056
comment: Phenotype [hp:0001742] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nasal obstruction
in dataset: phenotype

Atrial cardiomyopathy [hp:0200127]
type: SIO_010056
comment: Phenotype [hp:0200127] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atrial cardiomyopathy
in dataset: phenotype

Mildly reduced visual acuity [hp:0007739]
type: SIO_010056
comment: Phenotype [hp:0007739] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mildly reduced visual acuity
in dataset: phenotype

Exaggerated startle response [hp:0002267]
type: SIO_010056
comment: Phenotype [hp:0002267] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exaggerated startle response
in dataset: phenotype

Myopathy [hp:0003198]
type: SIO_010056
comment: Phenotype [hp:0003198] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myopathy
in dataset: phenotype

Low cholesterol esterification rates [hp:0003349]
type: SIO_010056
comment: Phenotype [hp:0003349] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low cholesterol esterification rates
in dataset: phenotype

Reduced renal corticomedullary differentiation [hp:0005565]
type: SIO_010056
comment: Phenotype [hp:0005565] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced renal corticomedullary differentiation
in dataset: phenotype

Spastic/hyperactive bladder [hp:0005340]
type: SIO_010056
comment: Phenotype [hp:0005340] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spastic/hyperactive bladder
in dataset: phenotype

Varus deformity of humeral neck [hp:0006362]
type: SIO_010056
comment: Phenotype [hp:0006362] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Varus deformity of humeral neck
in dataset: phenotype

Generalized aminoaciduria [hp:0002909]
type: SIO_010056
comment: Phenotype [hp:0002909] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized aminoaciduria
in dataset: phenotype

Protuberances at ends of long bones [hp:0003105]
type: SIO_010056
comment: Phenotype [hp:0003105] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Protuberances at ends of long bones
in dataset: phenotype

Age-dependent penetrance [hp:0003831]
type: SIO_010056
comment: Phenotype [hp:0003831] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Age-dependent penetrance
in dataset: phenotype

Deformed radius [hp:0003977]
type: SIO_010056
comment: Phenotype [hp:0003977] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deformed radius
in dataset: phenotype

Cartilaginous ossification of larynx [hp:0008747]
type: SIO_010056
comment: Phenotype [hp:0008747] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cartilaginous ossification of larynx
in dataset: phenotype

Tall lumbar vertebral bodies [hp:0008421]
type: SIO_010056
comment: Phenotype [hp:0008421] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tall lumbar vertebral bodies
in dataset: phenotype

Recurrent urinary tract infections [hp:0000010]
type: SIO_010056
comment: Phenotype [hp:0000010] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent urinary tract infections
in dataset: phenotype

Neoplasm of the breast [hp:0100013]
type: SIO_010056
comment: Phenotype [hp:0100013] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the breast
in dataset: phenotype

Benign gastrointestinal tract tumors [hp:0006719]
type: SIO_010056
comment: Phenotype [hp:0006719] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Benign gastrointestinal tract tumors
in dataset: phenotype

Redundant skin on fingers [hp:0007516]
type: SIO_010056
comment: Phenotype [hp:0007516] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Redundant skin on fingers
in dataset: phenotype

Decreased activity of mitochondrial respiratory chain [hp:0008972]
type: SIO_010056
comment: Phenotype [hp:0008972] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased activity of mitochondrial respiratory chain
in dataset: phenotype

Torticollis [hp:0000473]
type: SIO_010056
comment: Phenotype [hp:0000473] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Torticollis
in dataset: phenotype

Capitate-hamate fusion [hp:0001241]
type: SIO_010056
comment: Phenotype [hp:0001241] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Capitate-hamate fusion
in dataset: phenotype

3-4 toe syndactyly [hp:0009779]
type: SIO_010056
comment: Phenotype [hp:0009779] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 3-4 toe syndactyly
in dataset: phenotype

Low-set, posteriorly rotated ears [hp:0000368]
type: SIO_010056
comment: Phenotype [hp:0000368] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low-set, posteriorly rotated ears
in dataset: phenotype

Tongue telangiectasia [hp:0000227]
type: SIO_010056
comment: Phenotype [hp:0000227] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tongue telangiectasia
in dataset: phenotype

Abnormality of the spleen [hp:0001743]
type: SIO_010056
comment: Phenotype [hp:0001743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the spleen
in dataset: phenotype

Impaired thrombin-induced platelet aggregation [hp:0011872]
type: SIO_010056
comment: Phenotype [hp:0011872] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired thrombin-induced platelet aggregation
in dataset: phenotype

Mesocardia [hp:0011599]
type: SIO_010056
comment: Phenotype [hp:0011599] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mesocardia
in dataset: phenotype

Striae distensae [hp:0001065]
type: SIO_010056
comment: Phenotype [hp:0001065] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Striae distensae
in dataset: phenotype

Neoplasm of the parathyroid gland [hp:0100733]
type: SIO_010056
comment: Phenotype [hp:0100733] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the parathyroid gland
in dataset: phenotype

Female hypogonadism [hp:0000134]
type: SIO_010056
comment: Phenotype [hp:0000134] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Female hypogonadism
in dataset: phenotype

Syncope [hp:0001279]
type: SIO_010056
comment: Phenotype [hp:0001279] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Syncope
in dataset: phenotype

Abnormality of the sclera [hp:0000591]
type: SIO_010056
comment: Phenotype [hp:0000591] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the sclera
in dataset: phenotype

Retinal hypoplasia [hp:0007770]
type: SIO_010056
comment: Phenotype [hp:0007770] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal hypoplasia
in dataset: phenotype

Intestinal atresia [hp:0011100]
type: SIO_010056
comment: Phenotype [hp:0011100] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intestinal atresia
in dataset: phenotype

Flared metaphysis [hp:0003015]
type: SIO_010056
comment: Phenotype [hp:0003015] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flared metaphysis
in dataset: phenotype

Frontoparietal polymicrogyria [hp:0007095]
type: SIO_010056
comment: Phenotype [hp:0007095] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontoparietal polymicrogyria
in dataset: phenotype

Oroticaciduria [hp:0003218]
type: SIO_010056
comment: Phenotype [hp:0003218] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oroticaciduria
in dataset: phenotype

Cerebral cortical neurodegeneration [hp:0006964]
type: SIO_010056
comment: Phenotype [hp:0006964] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral cortical neurodegeneration
in dataset: phenotype

Papule [hp:0200034]
type: SIO_010056
comment: Phenotype [hp:0200034] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Papule
in dataset: phenotype

Broad hallux [hp:0010055]
type: SIO_010056
comment: Phenotype [hp:0010055] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad hallux
in dataset: phenotype

High maternal serum alpha-fetoprotein [hp:0011432]
type: SIO_010056
comment: Phenotype [hp:0011432] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High maternal serum alpha-fetoprotein
in dataset: phenotype

Intractable diarrhea [hp:0002041]
type: SIO_010056
comment: Phenotype [hp:0002041] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intractable diarrhea
in dataset: phenotype

Neuronal loss in basal ganglia [hp:0200147]
type: SIO_010056
comment: Phenotype [hp:0200147] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neuronal loss in basal ganglia
in dataset: phenotype

Cortically dense long tubular bones [hp:0006415]
type: SIO_010056
comment: Phenotype [hp:0006415] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cortically dense long tubular bones
in dataset: phenotype

Aplasia cutis congenita over the scalp vertex [hp:0004471]
type: SIO_010056
comment: Phenotype [hp:0004471] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia cutis congenita over the scalp vertex
in dataset: phenotype

Abnormal isoelectric focusing of serum transferrin [hp:0003160]
type: SIO_010056
comment: Phenotype [hp:0003160] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal isoelectric focusing of serum transferrin
in dataset: phenotype

Abnormality of the gallbladder [hp:0005264]
type: SIO_010056
comment: Phenotype [hp:0005264] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the gallbladder
in dataset: phenotype

Posterior fossa cyst [hp:0007291]
type: SIO_010056
comment: Phenotype [hp:0007291] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior fossa cyst
in dataset: phenotype

High-frequency sensorineural hearing impairment [hp:0001757]
type: SIO_010056
comment: Phenotype [hp:0001757] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High-frequency sensorineural hearing impairment
in dataset: phenotype

Brachycephaly [hp:0000248]
type: SIO_010056
comment: Phenotype [hp:0000248] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Brachycephaly
in dataset: phenotype

Vestibular hypofunction [hp:0001756]
type: SIO_010056
comment: Phenotype [hp:0001756] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vestibular hypofunction
in dataset: phenotype

Pancreatic fibrosis [hp:0100732]
type: SIO_010056
comment: Phenotype [hp:0100732] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pancreatic fibrosis
in dataset: phenotype

Hypogonadism [hp:0000135]
type: SIO_010056
comment: Phenotype [hp:0000135] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypogonadism
in dataset: phenotype

Neonatal unconjugated hyperbilirubinemia [hp:0008176]
type: SIO_010056
comment: Phenotype [hp:0008176] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neonatal unconjugated hyperbilirubinemia
in dataset: phenotype

Abnormality of the hairline [hp:0009553]
type: SIO_010056
comment: Phenotype [hp:0009553] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the hairline
in dataset: phenotype

Hypoplasia of the vagina [hp:0008726]
type: SIO_010056
comment: Phenotype [hp:0008726] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the vagina
in dataset: phenotype

Anterior wedging of L1 [hp:0008432]
type: SIO_010056
comment: Phenotype [hp:0008432] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior wedging of L1
in dataset: phenotype

Progressive external ophthalmoplegia [hp:0000590]
type: SIO_010056
comment: Phenotype [hp:0000590] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive external ophthalmoplegia
in dataset: phenotype

Metaphyseal widening [hp:0003016]
type: SIO_010056
comment: Phenotype [hp:0003016] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metaphyseal widening
in dataset: phenotype

Oncocytic cardiomyopathy [hp:0005152]
type: SIO_010056
comment: Phenotype [hp:0005152] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oncocytic cardiomyopathy
in dataset: phenotype

Acute necrotizing encephalopathy [hp:0006965]
type: SIO_010056
comment: Phenotype [hp:0006965] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute necrotizing encephalopathy
in dataset: phenotype

Abnormality of the first metatarsal bone [hp:0010054]
type: SIO_010056
comment: Phenotype [hp:0010054] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the first metatarsal bone
in dataset: phenotype

IgG deficiency [hp:0004315]
type: SIO_010056
comment: Phenotype [hp:0004315] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: IgG deficiency
in dataset: phenotype

Hyperglutaminemia [hp:0003217]
type: SIO_010056
comment: Phenotype [hp:0003217] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperglutaminemia
in dataset: phenotype

Gastritis [hp:0005263]
type: SIO_010056
comment: Phenotype [hp:0005263] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gastritis
in dataset: phenotype

4-Hydroxyphenylpyruvic aciduria [hp:0003161]
type: SIO_010056
comment: Phenotype [hp:0003161] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 4-Hydroxyphenylpyruvic aciduria
in dataset: phenotype

Mandibular hyperostosis [hp:0004472]
type: SIO_010056
comment: Phenotype [hp:0004472] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mandibular hyperostosis
in dataset: phenotype

Short femur [hp:0003097]
type: SIO_010056
comment: Phenotype [hp:0003097] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short femur
in dataset: phenotype

Tongue fasciculations [hp:0001308]
type: SIO_010056
comment: Phenotype [hp:0001308] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tongue fasciculations
in dataset: phenotype

Retinitis pigmentosa [hp:0000510]
type: SIO_010056
comment: Phenotype [hp:0000510] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinitis pigmentosa
in dataset: phenotype

Menorrhagia [hp:0000132]
type: SIO_010056
comment: Phenotype [hp:0000132] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Menorrhagia
in dataset: phenotype

Acrocyanosis [hp:0001063]
type: SIO_010056
comment: Phenotype [hp:0001063] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acrocyanosis
in dataset: phenotype

Paroxysmal choreoathetosis [hp:0007098]
type: SIO_010056
comment: Phenotype [hp:0007098] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paroxysmal choreoathetosis
in dataset: phenotype

Myotonia with warm-up phenomenon [hp:0003740]
type: SIO_010056
comment: Phenotype [hp:0003740] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myotonia with warm-up phenomenon
in dataset: phenotype

Perseveration [hp:0030223]
type: SIO_010056
comment: Phenotype [hp:0030223] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Perseveration
in dataset: phenotype

Distichiasis [hp:0009743]
type: SIO_010056
comment: Phenotype [hp:0009743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distichiasis
in dataset: phenotype

Reversed usual vertebral column curves [hp:0008433]
type: SIO_010056
comment: Phenotype [hp:0008433] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reversed usual vertebral column curves
in dataset: phenotype

Projection of scalp hair onto lateral cheek [hp:0009554]
type: SIO_010056
comment: Phenotype [hp:0009554] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Projection of scalp hair onto lateral cheek
in dataset: phenotype

Absence of labia majora [hp:0008729]
type: SIO_010056
comment: Phenotype [hp:0008729] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of labia majora
in dataset: phenotype

Ventricular escape rhythms [hp:0005155]
type: SIO_010056
comment: Phenotype [hp:0005155] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ventricular escape rhythms
in dataset: phenotype

Kayser-Fleischer ring [hp:0200032]
type: SIO_010056
comment: Phenotype [hp:0200032] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Kayser-Fleischer ring
in dataset: phenotype

Cranial nerve motor loss [hp:0007097]
type: SIO_010056
comment: Phenotype [hp:0007097] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cranial nerve motor loss
in dataset: phenotype

Long eyebrows [hp:0004523]
type: SIO_010056
comment: Phenotype [hp:0004523] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long eyebrows
in dataset: phenotype

Impaired smooth pursuit [hp:0007772]
type: SIO_010056
comment: Phenotype [hp:0007772] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired smooth pursuit
in dataset: phenotype

Hypertensive crisis [hp:0100735]
type: SIO_010056
comment: Phenotype [hp:0100735] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertensive crisis
in dataset: phenotype

Broad femoral metaphyses [hp:0006417]
type: SIO_010056
comment: Phenotype [hp:0006417] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad femoral metaphyses
in dataset: phenotype

Limited neck flexion [hp:0005991]
type: SIO_010056
comment: Phenotype [hp:0005991] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited neck flexion
in dataset: phenotype

Fasting hypoglycemia [hp:0003162]
type: SIO_010056
comment: Phenotype [hp:0003162] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fasting hypoglycemia
in dataset: phenotype

Gonadal dysgenesis [hp:0000133]
type: SIO_010056
comment: Phenotype [hp:0000133] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gonadal dysgenesis
in dataset: phenotype

Degenerative joint disease [hp:0001379]
type: SIO_010056
comment: Phenotype [hp:0001379] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Degenerative joint disease
in dataset: phenotype

Episodic hypersomnia [hp:0007200]
type: SIO_010056
comment: Phenotype [hp:0007200] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic hypersomnia
in dataset: phenotype

Vertical supranuclear gaze palsy [hp:0000511]
type: SIO_010056
comment: Phenotype [hp:0000511] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vertical supranuclear gaze palsy
in dataset: phenotype

Abnormality of vertebral epiphysis morphology [hp:0100734]
type: SIO_010056
comment: Phenotype [hp:0100734] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of vertebral epiphysis morphology
in dataset: phenotype

Sinusitis [hp:0000246]
type: SIO_010056
comment: Phenotype [hp:0000246] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sinusitis
in dataset: phenotype

Hypoplasia of the pharynx [hp:0009555]
type: SIO_010056
comment: Phenotype [hp:0009555] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the pharynx
in dataset: phenotype

Congenital muscular dystrophy [hp:0003741]
type: SIO_010056
comment: Phenotype [hp:0003741] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital muscular dystrophy
in dataset: phenotype

Stiff shoulders [hp:0009742]
type: SIO_010056
comment: Phenotype [hp:0009742] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stiff shoulders
in dataset: phenotype

Subcortical dementia [hp:0007123]
type: SIO_010056
comment: Phenotype [hp:0007123] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subcortical dementia
in dataset: phenotype

Orthostatic hypotension [hp:0001278]
type: SIO_010056
comment: Phenotype [hp:0001278] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Orthostatic hypotension
in dataset: phenotype

Hypoplastic cervical vertebrae [hp:0008434]
type: SIO_010056
comment: Phenotype [hp:0008434] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic cervical vertebrae
in dataset: phenotype

Esophageal varix [hp:0002040]
type: SIO_010056
comment: Phenotype [hp:0002040] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Esophageal varix
in dataset: phenotype

Anaphylactoid purpura [hp:0200144]
type: SIO_010056
comment: Phenotype [hp:0200144] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anaphylactoid purpura
in dataset: phenotype

Vitreoretinal abnormalities [hp:0007773]
type: SIO_010056
comment: Phenotype [hp:0007773] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vitreoretinal abnormalities
in dataset: phenotype

Ethylmalonic aciduria [hp:0003219]
type: SIO_010056
comment: Phenotype [hp:0003219] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ethylmalonic aciduria
in dataset: phenotype

Hypoplasia of the optic tract [hp:0007096]
type: SIO_010056
comment: Phenotype [hp:0007096] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the optic tract
in dataset: phenotype

Persistent open anterior fontanelle [hp:0004474]
type: SIO_010056
comment: Phenotype [hp:0004474] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Persistent open anterior fontanelle
in dataset: phenotype

Multiple rib fractures [hp:0006640]
type: SIO_010056
comment: Phenotype [hp:0006640] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple rib fractures
in dataset: phenotype

Neoplasm of the stomach [hp:0006753]
type: SIO_010056
comment: Phenotype [hp:0006753] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the stomach
in dataset: phenotype

Joint hemorrhage [hp:0005261]
type: SIO_010056
comment: Phenotype [hp:0005261] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Joint hemorrhage
in dataset: phenotype

Thyroid hypoplasia [hp:0005990]
type: SIO_010056
comment: Phenotype [hp:0005990] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thyroid hypoplasia
in dataset: phenotype

Elevated urinary delta-aminolevulinic acid [hp:0003163]
type: SIO_010056
comment: Phenotype [hp:0003163] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated urinary delta-aminolevulinic acid
in dataset: phenotype

Prominent metopic ridge [hp:0005487]
type: SIO_010056
comment: Phenotype [hp:0005487] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent metopic ridge
in dataset: phenotype

Septic arthritis [hp:0003095]
type: SIO_010056
comment: Phenotype [hp:0003095] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Septic arthritis
in dataset: phenotype

Prominent crus of helix [hp:0009899]
type: SIO_010056
comment: Phenotype [hp:0009899] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent crus of helix
in dataset: phenotype

Abnormality of the uterus [hp:0000130]
type: SIO_010056
comment: Phenotype [hp:0000130] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the uterus
in dataset: phenotype

Absent tibia [hp:0009556]
type: SIO_010056
comment: Phenotype [hp:0009556] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent tibia
in dataset: phenotype

Episodic hyperhidrosis [hp:0001069]
type: SIO_010056
comment: Phenotype [hp:0001069] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic hyperhidrosis
in dataset: phenotype

Limitation of joint mobility [hp:0001376]
type: SIO_010056
comment: Phenotype [hp:0001376] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limitation of joint mobility
in dataset: phenotype

Abnormal electroretinogram [hp:0000512]
type: SIO_010056
comment: Phenotype [hp:0000512] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal electroretinogram
in dataset: phenotype

Limited hip extension [hp:0003093]
type: SIO_010056
comment: Phenotype [hp:0003093] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited hip extension
in dataset: phenotype

Abnormality of the musculature [hp:0003011]
type: SIO_010056
comment: Phenotype [hp:0003011] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the musculature
in dataset: phenotype

Hypothalamic gonadotropin-releasing hormone (GNRH) deficiency [hp:0003164]
type: SIO_010056
comment: Phenotype [hp:0003164] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypothalamic gonadotropin-releasing hormone (GNRH) deficiency
in dataset: phenotype

Prolonged G2 phase of cell cycle [hp:0003214]
type: SIO_010056
comment: Phenotype [hp:0003214] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolonged G2 phase of cell cycle
in dataset: phenotype

Punctate vasculitis skin lesions [hp:0200030]
type: SIO_010056
comment: Phenotype [hp:0200030] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Punctate vasculitis skin lesions
in dataset: phenotype

Chondroitin sulfate excretion in urine [hp:0012070]
type: SIO_010056
comment: Phenotype [hp:0012070] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chondroitin sulfate excretion in urine
in dataset: phenotype

Hypoplasia of the ciliary body [hp:0007774]
type: SIO_010056
comment: Phenotype [hp:0007774] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the ciliary body
in dataset: phenotype

Transient ischemic attack [hp:0002326]
type: SIO_010056
comment: Phenotype [hp:0002326] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Transient ischemic attack
in dataset: phenotype

Uterine leiomyoma [hp:0000131]
type: SIO_010056
comment: Phenotype [hp:0000131] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Uterine leiomyoma
in dataset: phenotype

Muscular hypotonia of the trunk [hp:0008936]
type: SIO_010056
comment: Phenotype [hp:0008936] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscular hypotonia of the trunk
in dataset: phenotype

Deviation of the 5th finger [hp:0009179]
type: SIO_010056
comment: Phenotype [hp:0009179] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deviation of the 5th finger
in dataset: phenotype

Spontaneous hematomas [hp:0007420]
type: SIO_010056
comment: Phenotype [hp:0007420] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spontaneous hematomas
in dataset: phenotype

Limited elbow extension [hp:0001377]
type: SIO_010056
comment: Phenotype [hp:0001377] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited elbow extension
in dataset: phenotype

Large earlobe [hp:0009748]
type: SIO_010056
comment: Phenotype [hp:0009748] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large earlobe
in dataset: phenotype

Shallow anterior chamber [hp:0000594]
type: SIO_010056
comment: Phenotype [hp:0000594] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shallow anterior chamber
in dataset: phenotype

Death in infancy [hp:0001522]
type: SIO_010056
comment: Phenotype [hp:0001522] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Death in infancy
in dataset: phenotype

Increased mean platelet volume [hp:0011877]
type: SIO_010056
comment: Phenotype [hp:0011877] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased mean platelet volume
in dataset: phenotype

Phosphoethanolaminuria [hp:0003239]
type: SIO_010056
comment: Phenotype [hp:0003239] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Phosphoethanolaminuria
in dataset: phenotype

Elevated circulating parathyroid hormone (PTH) level [hp:0003165]
type: SIO_010056
comment: Phenotype [hp:0003165] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated circulating parathyroid hormone (PTH) level
in dataset: phenotype

Periorbital edema [hp:0100539]
type: SIO_010056
comment: Phenotype [hp:0100539] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Periorbital edema
in dataset: phenotype

Abnormality of the soft palate [hp:0100736]
type: SIO_010056
comment: Phenotype [hp:0100736] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the soft palate
in dataset: phenotype

Deficient excision of UV-induced pyrimidine dimers in DNA [hp:0003213]
type: SIO_010056
comment: Phenotype [hp:0003213] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deficient excision of UV-induced pyrimidine dimers in DNA
in dataset: phenotype

Temporal hypotrichosis [hp:0004524]
type: SIO_010056
comment: Phenotype [hp:0004524] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Temporal hypotrichosis
in dataset: phenotype

Akinetic mutism [hp:0012672]
type: SIO_010056
comment: Phenotype [hp:0012672] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Akinetic mutism
in dataset: phenotype

Cutaneous leiomyosarcoma [hp:0006755]
type: SIO_010056
comment: Phenotype [hp:0006755] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cutaneous leiomyosarcoma
in dataset: phenotype

Hypoaldosteronism [hp:0004319]
type: SIO_010056
comment: Phenotype [hp:0004319] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoaldosteronism
in dataset: phenotype

Reticulate pigmentation of oral mucosa [hp:0012788]
type: SIO_010056
comment: Phenotype [hp:0012788] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reticulate pigmentation of oral mucosa
in dataset: phenotype

EEG with generalized slow activity [hp:0010845]
type: SIO_010056
comment: Phenotype [hp:0010845] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EEG with generalized slow activity
in dataset: phenotype

Congenital hip dislocation [hp:0001374]
type: SIO_010056
comment: Phenotype [hp:0001374] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital hip dislocation
in dataset: phenotype

Neurofibromas [hp:0001067]
type: SIO_010056
comment: Phenotype [hp:0001067] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neurofibromas
in dataset: phenotype

Abnormality of the anterior chamber [hp:0000593]
type: SIO_010056
comment: Phenotype [hp:0000593] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the anterior chamber
in dataset: phenotype

Abnormal atrioventricular conduction [hp:0005150]
type: SIO_010056
comment: Phenotype [hp:0005150] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal atrioventricular conduction
in dataset: phenotype

Short hard palate [hp:0010290]
type: SIO_010056
comment: Phenotype [hp:0010290] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short hard palate
in dataset: phenotype

Proximal amyotrophy [hp:0007126]
type: SIO_010056
comment: Phenotype [hp:0007126] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal amyotrophy
in dataset: phenotype

Median cleft lip and palate [hp:0008501]
type: SIO_010056
comment: Phenotype [hp:0008501] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Median cleft lip and palate
in dataset: phenotype

Telangiectases of the cheeks [hp:0007421]
type: SIO_010056
comment: Phenotype [hp:0007421] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Telangiectases of the cheeks
in dataset: phenotype

Lumbosacral hirsutism [hp:0009747]
type: SIO_010056
comment: Phenotype [hp:0009747] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lumbosacral hirsutism
in dataset: phenotype

Increased urinary taurine [hp:0003166]
type: SIO_010056
comment: Phenotype [hp:0003166] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased urinary taurine
in dataset: phenotype

Postnatal microcephaly [hp:0005484]
type: SIO_010056
comment: Phenotype [hp:0005484] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Postnatal microcephaly
in dataset: phenotype

Prominent nose [hp:0000448]
type: SIO_010056
comment: Phenotype [hp:0000448] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent nose
in dataset: phenotype

Rod monochromacy [hp:0011516]
type: SIO_010056
comment: Phenotype [hp:0011516] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rod monochromacy
in dataset: phenotype

Bulging epiphyses [hp:0003013]
type: SIO_010056
comment: Phenotype [hp:0003013] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bulging epiphyses
in dataset: phenotype

CSF lymphocytic pleiocytosis [hp:0200149]
type: SIO_010056
comment: Phenotype [hp:0200149] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: CSF lymphocytic pleiocytosis
in dataset: phenotype

Slow saccadic eye movements [hp:0000514]
type: SIO_010056
comment: Phenotype [hp:0000514] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slow saccadic eye movements
in dataset: phenotype

Aciduria [hp:0012072]
type: SIO_010056
comment: Phenotype [hp:0012072] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aciduria
in dataset: phenotype

Drowsiness [hp:0002329]
type: SIO_010056
comment: Phenotype [hp:0002329] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Drowsiness
in dataset: phenotype

Fifth metacarpal with ulnar notch [hp:0005900]
type: SIO_010056
comment: Phenotype [hp:0005900] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fifth metacarpal with ulnar notch
in dataset: phenotype

Large clumps of pigment irregularly distributed along hair shaft [hp:0004527]
type: SIO_010056
comment: Phenotype [hp:0004527] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large clumps of pigment irregularly distributed along hair shaft
in dataset: phenotype

Generalized amyloid deposition [hp:0003216]
type: SIO_010056
comment: Phenotype [hp:0003216] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized amyloid deposition
in dataset: phenotype

Sparse lower eyelashes [hp:0007776]
type: SIO_010056
comment: Phenotype [hp:0007776] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sparse lower eyelashes
in dataset: phenotype

Diffuse leiomyomatosis [hp:0006756]
type: SIO_010056
comment: Phenotype [hp:0006756] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse leiomyomatosis
in dataset: phenotype

Preductal coarctation of the aorta [hp:0005151]
type: SIO_010056
comment: Phenotype [hp:0005151] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Preductal coarctation of the aorta
in dataset: phenotype

Decreased adipose tissue around neck [hp:0005995]
type: SIO_010056
comment: Phenotype [hp:0005995] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased adipose tissue around neck
in dataset: phenotype

Underfolded superior helices [hp:0008583]
type: SIO_010056
comment: Phenotype [hp:0008583] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Underfolded superior helices
in dataset: phenotype

Proximal/middle symphalangism of 5th finger [hp:0009177]
type: SIO_010056
comment: Phenotype [hp:0009177] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal/middle symphalangism of 5th finger
in dataset: phenotype

Blue sclerae [hp:0000592]
type: SIO_010056
comment: Phenotype [hp:0000592] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Blue sclerae
in dataset: phenotype

Anterior beaking of lumbar vertebrae [hp:0008430]
type: SIO_010056
comment: Phenotype [hp:0008430] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior beaking of lumbar vertebrae
in dataset: phenotype

Hypoplasia of the ovary [hp:0008724]
type: SIO_010056
comment: Phenotype [hp:0008724] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the ovary
in dataset: phenotype

Large for gestational age [hp:0001520]
type: SIO_010056
comment: Phenotype [hp:0001520] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large for gestational age
in dataset: phenotype

Hypoplasia of the capital femoral epiphysis [hp:0003090]
type: SIO_010056
comment: Phenotype [hp:0003090] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the capital femoral epiphysis
in dataset: phenotype

Thick nasal septum [hp:0009746]
type: SIO_010056
comment: Phenotype [hp:0009746] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thick nasal septum
in dataset: phenotype

Pear-shaped nose [hp:0000447]
type: SIO_010056
comment: Phenotype [hp:0000447] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pear-shaped nose
in dataset: phenotype

Abnormal eating behavior [hp:0100738]
type: SIO_010056
comment: Phenotype [hp:0100738] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal eating behavior
in dataset: phenotype

Abnormal stereopsis [hp:0011515]
type: SIO_010056
comment: Phenotype [hp:0011515] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal stereopsis
in dataset: phenotype

Carnosinuria [hp:0003167]
type: SIO_010056
comment: Phenotype [hp:0003167] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Carnosinuria
in dataset: phenotype

Nodular goiter [hp:0005994]
type: SIO_010056
comment: Phenotype [hp:0005994] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nodular goiter
in dataset: phenotype

Distal tibial bowing [hp:0006414]
type: SIO_010056
comment: Phenotype [hp:0006414] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal tibial bowing
in dataset: phenotype

Abnormal liver function tests during pregnancy [hp:0200148]
type: SIO_010056
comment: Phenotype [hp:0200148] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal liver function tests during pregnancy
in dataset: phenotype

Increased IgG level [hp:0003237]
type: SIO_010056
comment: Phenotype [hp:0003237] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased IgG level
in dataset: phenotype

Anisospondyly [hp:0002879]
type: SIO_010056
comment: Phenotype [hp:0002879] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anisospondyly
in dataset: phenotype

Alopecia areata [hp:0002229]
type: SIO_010056
comment: Phenotype [hp:0002229] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Alopecia areata
in dataset: phenotype

Abnormality of the pulmonary veins [hp:0011718]
type: SIO_010056
comment: Phenotype [hp:0011718] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the pulmonary veins
in dataset: phenotype

Chronic recurrent multifocal osteomyelitis [hp:0005901]
type: SIO_010056
comment: Phenotype [hp:0005901] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic recurrent multifocal osteomyelitis
in dataset: phenotype

Generalized osteosclerosis [hp:0005789]
type: SIO_010056
comment: Phenotype [hp:0005789] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized osteosclerosis
in dataset: phenotype

Dicarboxylic aciduria [hp:0003215]
type: SIO_010056
comment: Phenotype [hp:0003215] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dicarboxylic aciduria
in dataset: phenotype

Thin clavicles [hp:0006645]
type: SIO_010056
comment: Phenotype [hp:0006645] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thin clavicles
in dataset: phenotype

Posterior leukoencephalopathy [hp:0006859]
type: SIO_010056
comment: Phenotype [hp:0006859] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior leukoencephalopathy
in dataset: phenotype

Tonic pupil [hp:0012074]
type: SIO_010056
comment: Phenotype [hp:0012074] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tonic pupil
in dataset: phenotype

Curly eyelashes [hp:0007665]
type: SIO_010056
comment: Phenotype [hp:0007665] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Curly eyelashes
in dataset: phenotype

Delayed gross motor development [hp:0002194]
type: SIO_010056
comment: Phenotype [hp:0002194] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed gross motor development
in dataset: phenotype

Progressive pulmonary function impairment [hp:0006520]
type: SIO_010056
comment: Phenotype [hp:0006520] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive pulmonary function impairment
in dataset: phenotype

Neovascularization of peripheral and posterior retina [hp:0007778]
type: SIO_010056
comment: Phenotype [hp:0007778] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neovascularization of peripheral and posterior retina
in dataset: phenotype

Generalized hyperkeratosis [hp:0005595]
type: SIO_010056
comment: Phenotype [hp:0005595] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized hyperkeratosis
in dataset: phenotype

Diarrhea [hp:0002014]
type: SIO_010056
comment: Phenotype [hp:0002014] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diarrhea
in dataset: phenotype

Proximal renal tubular acidosis [hp:0002049]
type: SIO_010056
comment: Phenotype [hp:0002049] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal renal tubular acidosis
in dataset: phenotype

Inappropriate behavior [hp:0000719]
type: SIO_010056
comment: Phenotype [hp:0000719] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inappropriate behavior
in dataset: phenotype

Undulate ribs [hp:0010561]
type: SIO_010056
comment: Phenotype [hp:0010561] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Undulate ribs
in dataset: phenotype

Hypokalemia [hp:0002900]
type: SIO_010056
comment: Phenotype [hp:0002900] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypokalemia
in dataset: phenotype

Macrocytic anemia [hp:0001972]
type: SIO_010056
comment: Phenotype [hp:0001972] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macrocytic anemia
in dataset: phenotype

Ectrodactyly [hp:0100257]
type: SIO_010056
comment: Phenotype [hp:0100257] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectrodactyly
in dataset: phenotype

Adipose tissue loss [hp:0008887]
type: SIO_010056
comment: Phenotype [hp:0008887] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adipose tissue loss
in dataset: phenotype

Urethral stenosis [hp:0008661]
type: SIO_010056
comment: Phenotype [hp:0008661] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urethral stenosis
in dataset: phenotype

Micromelia [hp:0002983]
type: SIO_010056
comment: Phenotype [hp:0002983] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Micromelia
in dataset: phenotype

Otitis media [hp:0000388]
type: SIO_010056
comment: Phenotype [hp:0000388] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Otitis media
in dataset: phenotype

Short clavicles [hp:0000894]
type: SIO_010056
comment: Phenotype [hp:0000894] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short clavicles
in dataset: phenotype

Ivory epiphyses [hp:0010583]
type: SIO_010056
comment: Phenotype [hp:0010583] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ivory epiphyses
in dataset: phenotype

Occipital meningocele [hp:0002436]
type: SIO_010056
comment: Phenotype [hp:0002436] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Occipital meningocele
in dataset: phenotype

Atrophic, patchy alopecia [hp:0004529]
type: SIO_010056
comment: Phenotype [hp:0004529] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atrophic, patchy alopecia
in dataset: phenotype

Elevated imprint of the transverse sinuses [hp:0000930]
type: SIO_010056
comment: Phenotype [hp:0000930] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated imprint of the transverse sinuses
in dataset: phenotype

Cutaneous syndactyly of toes [hp:0010621]
type: SIO_010056
comment: Phenotype [hp:0010621] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cutaneous syndactyly of toes
in dataset: phenotype

Anencephaly [hp:0002323]
type: SIO_010056
comment: Phenotype [hp:0002323] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anencephaly
in dataset: phenotype

Personality disorder [hp:0012075]
type: SIO_010056
comment: Phenotype [hp:0012075] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Personality disorder
in dataset: phenotype

Costal cartilage calcification [hp:0006646]
type: SIO_010056
comment: Phenotype [hp:0006646] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Costal cartilage calcification
in dataset: phenotype

Dysgenesis of the cerebellar vermis [hp:0002195]
type: SIO_010056
comment: Phenotype [hp:0002195] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysgenesis of the cerebellar vermis
in dataset: phenotype

Pulmonary lymphangiectasia [hp:0006521]
type: SIO_010056
comment: Phenotype [hp:0006521] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary lymphangiectasia
in dataset: phenotype

Laryngotracheal stenosis [hp:0004894]
type: SIO_010056
comment: Phenotype [hp:0004894] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laryngotracheal stenosis
in dataset: phenotype

Type B brachydactyly [hp:0005831]
type: SIO_010056
comment: Phenotype [hp:0005831] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type B brachydactyly
in dataset: phenotype

Vomiting [hp:0002013]
type: SIO_010056
comment: Phenotype [hp:0002013] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vomiting
in dataset: phenotype

Anterior segment of eye aplasia [hp:0007779]
type: SIO_010056
comment: Phenotype [hp:0007779] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior segment of eye aplasia
in dataset: phenotype

Hyperreflexia in upper limbs [hp:0007350]
type: SIO_010056
comment: Phenotype [hp:0007350] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperreflexia in upper limbs
in dataset: phenotype

White eyelashes [hp:0002227]
type: SIO_010056
comment: Phenotype [hp:0002227] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: White eyelashes
in dataset: phenotype

Hypocalcemia [hp:0002901]
type: SIO_010056
comment: Phenotype [hp:0002901] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypocalcemia
in dataset: phenotype

Aggressive behavior [hp:0000718]
type: SIO_010056
comment: Phenotype [hp:0000718] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aggressive behavior
in dataset: phenotype

3-4 finger cutaneous syndactyly [hp:0011939]
type: SIO_010056
comment: Phenotype [hp:0011939] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 3-4 finger cutaneous syndactyly
in dataset: phenotype

Keloids [hp:0010562]
type: SIO_010056
comment: Phenotype [hp:0010562] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Keloids
in dataset: phenotype

Chronic otitis media [hp:0000389]
type: SIO_010056
comment: Phenotype [hp:0000389] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic otitis media
in dataset: phenotype

Defect in the atrial septum [hp:0001631]
type: SIO_010056
comment: Phenotype [hp:0001631] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Defect in the atrial septum
in dataset: phenotype

Abnormality of the ear [hp:0000598]
type: SIO_010056
comment: Phenotype [hp:0000598] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the ear
in dataset: phenotype

Tibial bowing [hp:0002982]
type: SIO_010056
comment: Phenotype [hp:0002982] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tibial bowing
in dataset: phenotype

Preaxial polydactyly [hp:0100258]
type: SIO_010056
comment: Phenotype [hp:0100258] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Preaxial polydactyly
in dataset: phenotype

Autoimmune thrombocytopenia [hp:0001973]
type: SIO_010056
comment: Phenotype [hp:0001973] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autoimmune thrombocytopenia
in dataset: phenotype

Upper limb postural tremor [hp:0007351]
type: SIO_010056
comment: Phenotype [hp:0007351] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Upper limb postural tremor
in dataset: phenotype

Pseudoepiphyses [hp:0010584]
type: SIO_010056
comment: Phenotype [hp:0010584] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pseudoepiphyses
in dataset: phenotype

Meningocele [hp:0002435]
type: SIO_010056
comment: Phenotype [hp:0002435] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Meningocele
in dataset: phenotype

Bulging of the costochondral junction [hp:0000893]
type: SIO_010056
comment: Phenotype [hp:0000893] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bulging of the costochondral junction
in dataset: phenotype

Resting tremor [hp:0002322]
type: SIO_010056
comment: Phenotype [hp:0002322] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Resting tremor
in dataset: phenotype

Thinning and bulging of the posterior fossa bones [hp:0000931]
type: SIO_010056
comment: Phenotype [hp:0000931] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thinning and bulging of the posterior fossa bones
in dataset: phenotype

Malar prominence [hp:0010620]
type: SIO_010056
comment: Phenotype [hp:0010620] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malar prominence
in dataset: phenotype

Late onset congenital glaucoma [hp:0008041]
type: SIO_010056
comment: Phenotype [hp:0008041] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Late onset congenital glaucoma
in dataset: phenotype

Increased red cell osmotic fragility [hp:0005502]
type: SIO_010056
comment: Phenotype [hp:0005502] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased red cell osmotic fragility
in dataset: phenotype

Abnormality of the abdominal organs [hp:0002012]
type: SIO_010056
comment: Phenotype [hp:0002012] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the abdominal organs
in dataset: phenotype

Aplasia of the optic tract [hp:0010999]
type: SIO_010056
comment: Phenotype [hp:0010999] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the optic tract
in dataset: phenotype

Recurrent infections due to aspiration [hp:0004891]
type: SIO_010056
comment: Phenotype [hp:0004891] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent infections due to aspiration
in dataset: phenotype

Irregular, rachitic-like metaphyses [hp:0005042]
type: SIO_010056
comment: Phenotype [hp:0005042] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular, rachitic-like metaphyses
in dataset: phenotype

Episodic hemolytic anemia [hp:0004802]
type: SIO_010056
comment: Phenotype [hp:0004802] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic hemolytic anemia
in dataset: phenotype

Hyponatremia [hp:0002902]
type: SIO_010056
comment: Phenotype [hp:0002902] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyponatremia
in dataset: phenotype

Malignant hyperthermia [hp:0002047]
type: SIO_010056
comment: Phenotype [hp:0002047] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malignant hyperthermia
in dataset: phenotype

Cataract [hp:0000518]
type: SIO_010056
comment: Phenotype [hp:0000518] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cataract
in dataset: phenotype

Cystic retinal degeneration [hp:0007667]
type: SIO_010056
comment: Phenotype [hp:0007667] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cystic retinal degeneration
in dataset: phenotype

White eyebrow [hp:0002226]
type: SIO_010056
comment: Phenotype [hp:0002226] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: White eyebrow
in dataset: phenotype

Renal sarcoma [hp:0008663]
type: SIO_010056
comment: Phenotype [hp:0008663] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal sarcoma
in dataset: phenotype

Cerebellar calcifications [hp:0007352]
type: SIO_010056
comment: Phenotype [hp:0007352] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebellar calcifications
in dataset: phenotype

Leukocytosis [hp:0001974]
type: SIO_010056
comment: Phenotype [hp:0001974] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Leukocytosis
in dataset: phenotype

Ophthalmoparesis [hp:0000597]
type: SIO_010056
comment: Phenotype [hp:0000597] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ophthalmoparesis
in dataset: phenotype

Metaphyseal dysplasia [hp:0100255]
type: SIO_010056
comment: Phenotype [hp:0100255] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metaphyseal dysplasia
in dataset: phenotype

Eye poking [hp:0001483]
type: SIO_010056
comment: Phenotype [hp:0001483] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Eye poking
in dataset: phenotype

Hypoplasia of the cochlea [hp:0008586]
type: SIO_010056
comment: Phenotype [hp:0008586] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the cochlea
in dataset: phenotype

Small epiphyses [hp:0010585]
type: SIO_010056
comment: Phenotype [hp:0010585] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small epiphyses
in dataset: phenotype

Bifid ribs [hp:0000892]
type: SIO_010056
comment: Phenotype [hp:0000892] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid ribs
in dataset: phenotype

Progressive spasticity [hp:0002191]
type: SIO_010056
comment: Phenotype [hp:0002191] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive spasticity
in dataset: phenotype

Absent forearm [hp:0005632]
type: SIO_010056
comment: Phenotype [hp:0005632] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent forearm
in dataset: phenotype

Joint swelling onset late infancy [hp:0005833]
type: SIO_010056
comment: Phenotype [hp:0005833] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Joint swelling onset late infancy
in dataset: phenotype

Pseudobulbar behavioral symptoms [hp:0002193]
type: SIO_010056
comment: Phenotype [hp:0002193] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pseudobulbar behavioral symptoms
in dataset: phenotype

Pelvic girdle muscle weakness [hp:0003749]
type: SIO_010056
comment: Phenotype [hp:0003749] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pelvic girdle muscle weakness
in dataset: phenotype

Morphological abnormality of the central nervous system [hp:0002011]
type: SIO_010056
comment: Phenotype [hp:0002011] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Morphological abnormality of the central nervous system
in dataset: phenotype

Irregular capital femoral epiphysis [hp:0005041]
type: SIO_010056
comment: Phenotype [hp:0005041] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular capital femoral epiphysis
in dataset: phenotype

Prolonged bleeding time [hp:0003010]
type: SIO_010056
comment: Phenotype [hp:0003010] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolonged bleeding time
in dataset: phenotype

Giant melanosomes in melanocytes [hp:0005592]
type: SIO_010056
comment: Phenotype [hp:0005592] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Giant melanosomes in melanocytes
in dataset: phenotype

Congenital cataract [hp:0000519]
type: SIO_010056
comment: Phenotype [hp:0000519] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital cataract
in dataset: phenotype

Palmoplantar pustulosis [hp:0100847]
type: SIO_010056
comment: Phenotype [hp:0100847] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palmoplantar pustulosis
in dataset: phenotype

Pustule [hp:0200039]
type: SIO_010056
comment: Phenotype [hp:0200039] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pustule
in dataset: phenotype

Sparse pubic hair [hp:0002225]
type: SIO_010056
comment: Phenotype [hp:0002225] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sparse pubic hair
in dataset: phenotype

Renal cortical atrophy [hp:0002048]
type: SIO_010056
comment: Phenotype [hp:0002048] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal cortical atrophy
in dataset: phenotype

Congenital onset [hp:0003577]
type: SIO_010056
comment: Phenotype [hp:0003577] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital onset
in dataset: phenotype

Impaired pursuit initiation and maintenance [hp:0007668]
type: SIO_010056
comment: Phenotype [hp:0007668] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired pursuit initiation and maintenance
in dataset: phenotype

X-linked recessive inheritance [hp:0001419]
type: SIO_010056
comment: Phenotype [hp:0001419] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: X-linked recessive inheritance
in dataset: phenotype

Absent earlobe [hp:0000387]
type: SIO_010056
comment: Phenotype [hp:0000387] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent earlobe
in dataset: phenotype

Decreased platelet glycoprotein IIb-IIIa [hp:0001975]
type: SIO_010056
comment: Phenotype [hp:0001975] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased platelet glycoprotein IIb-IIIa
in dataset: phenotype

Senile plaques [hp:0100256]
type: SIO_010056
comment: Phenotype [hp:0100256] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Senile plaques
in dataset: phenotype

Undulate clavicles [hp:0010560]
type: SIO_010056
comment: Phenotype [hp:0010560] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Undulate clavicles
in dataset: phenotype

Hydranencephaly [hp:0002324]
type: SIO_010056
comment: Phenotype [hp:0002324] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hydranencephaly
in dataset: phenotype

Neoplasm of the skeletal system [hp:0010622]
type: SIO_010056
comment: Phenotype [hp:0010622] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the skeletal system
in dataset: phenotype

Vascular ring [hp:0010775]
type: SIO_010056
comment: Phenotype [hp:0010775] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vascular ring
in dataset: phenotype

Cervical ribs [hp:0000891]
type: SIO_010056
comment: Phenotype [hp:0000891] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cervical ribs
in dataset: phenotype

Mild neurosensory hearing impairment [hp:0008587]
type: SIO_010056
comment: Phenotype [hp:0008587] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mild neurosensory hearing impairment
in dataset: phenotype

Femoral bowing [hp:0002980]
type: SIO_010056
comment: Phenotype [hp:0002980] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Femoral bowing
in dataset: phenotype

Tracheobronchial leiomyomatosis [hp:0006524]
type: SIO_010056
comment: Phenotype [hp:0006524] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tracheobronchial leiomyomatosis
in dataset: phenotype

Radially deviated wrists [hp:0006190]
type: SIO_010056
comment: Phenotype [hp:0006190] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Radially deviated wrists
in dataset: phenotype

Hyperbilirubinemia [hp:0002904]
type: SIO_010056
comment: Phenotype [hp:0002904] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperbilirubinemia
in dataset: phenotype

Decreased plasma total carnitine [hp:0011936]
type: SIO_010056
comment: Phenotype [hp:0011936] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased plasma total carnitine
in dataset: phenotype

Motor conduction block [hp:0012078]
type: SIO_010056
comment: Phenotype [hp:0012078] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Motor conduction block
in dataset: phenotype

Woolly hair [hp:0002224]
type: SIO_010056
comment: Phenotype [hp:0002224] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Woolly hair
in dataset: phenotype

Hypothermia [hp:0002045]
type: SIO_010056
comment: Phenotype [hp:0002045] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypothermia
in dataset: phenotype

Chondrocalcinosis [hp:0000934]
type: SIO_010056
comment: Phenotype [hp:0000934] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chondrocalcinosis
in dataset: phenotype

Cleft of chin [hp:0011323]
type: SIO_010056
comment: Phenotype [hp:0011323] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cleft of chin
in dataset: phenotype

Broad hallux phalanx [hp:0010059]
type: SIO_010056
comment: Phenotype [hp:0010059] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad hallux phalanx
in dataset: phenotype

Dilated fourth ventricle [hp:0002198]
type: SIO_010056
comment: Phenotype [hp:0002198] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dilated fourth ventricle
in dataset: phenotype

Chorioretinal hypopigmentation or hyperpigmentation [hp:0007661]
type: SIO_010056
comment: Phenotype [hp:0007661] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chorioretinal hypopigmentation or hyperpigmentation
in dataset: phenotype

Chromosomal breakage induced by ionizing radiation [hp:0010997]
type: SIO_010056
comment: Phenotype [hp:0010997] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chromosomal breakage induced by ionizing radiation
in dataset: phenotype

Cerebellar vermis atrophy [hp:0006855]
type: SIO_010056
comment: Phenotype [hp:0006855] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebellar vermis atrophy
in dataset: phenotype

Narrow maxilla [hp:0002010]
type: SIO_010056
comment: Phenotype [hp:0002010] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow maxilla
in dataset: phenotype

Hypopigmentation of hair [hp:0005599]
type: SIO_010056
comment: Phenotype [hp:0005599] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypopigmentation of hair
in dataset: phenotype

Megaloblastic erythroid hyperplasia [hp:0200143]
type: SIO_010056
comment: Phenotype [hp:0200143] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Megaloblastic erythroid hyperplasia
in dataset: phenotype

Slit-like opening of the exterior auditory meatus [hp:0008588]
type: SIO_010056
comment: Phenotype [hp:0008588] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slit-like opening of the exterior auditory meatus
in dataset: phenotype

Reticulated skin pigmentation [hp:0007427]
type: SIO_010056
comment: Phenotype [hp:0007427] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reticulated skin pigmentation
in dataset: phenotype

Preauricular skin tag [hp:0000384]
type: SIO_010056
comment: Phenotype [hp:0000384] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Preauricular skin tag
in dataset: phenotype

Elbow flexion contracture [hp:0002987]
type: SIO_010056
comment: Phenotype [hp:0002987] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elbow flexion contracture
in dataset: phenotype

Septo-optic dysplasia [hp:0100842]
type: SIO_010056
comment: Phenotype [hp:0100842] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Septo-optic dysplasia
in dataset: phenotype

Mild intrauterine growth retardation [hp:0008883]
type: SIO_010056
comment: Phenotype [hp:0008883] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mild intrauterine growth retardation
in dataset: phenotype

Drusen [hp:0011510]
type: SIO_010056
comment: Phenotype [hp:0011510] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Drusen
in dataset: phenotype

Ovarian cyst [hp:0000138]
type: SIO_010056
comment: Phenotype [hp:0000138] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ovarian cyst
in dataset: phenotype

Amyotrophic lateral sclerosis [hp:0007354]
type: SIO_010056
comment: Phenotype [hp:0007354] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Amyotrophic lateral sclerosis
in dataset: phenotype

Reduced antithrombin III activity [hp:0001976]
type: SIO_010056
comment: Phenotype [hp:0001976] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced antithrombin III activity
in dataset: phenotype

Acne [hp:0001061]
type: SIO_010056
comment: Phenotype [hp:0001061] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acne
in dataset: phenotype

Long clavicles [hp:0000890]
type: SIO_010056
comment: Phenotype [hp:0000890] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long clavicles
in dataset: phenotype

Trigonocephaly [hp:0000243]
type: SIO_010056
comment: Phenotype [hp:0000243] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Trigonocephaly
in dataset: phenotype

Vitreous detachment [hp:0001489]
type: SIO_010056
comment: Phenotype [hp:0001489] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vitreous detachment
in dataset: phenotype

X-linked inheritance [hp:0001417]
type: SIO_010056
comment: Phenotype [hp:0001417] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: X-linked inheritance
in dataset: phenotype

Hyperphosphatemia [hp:0002905]
type: SIO_010056
comment: Phenotype [hp:0002905] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperphosphatemia
in dataset: phenotype

Abnormal thrombosis [hp:0001977]
type: SIO_010056
comment: Phenotype [hp:0001977] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal thrombosis
in dataset: phenotype

Skin vesicle [hp:0200037]
type: SIO_010056
comment: Phenotype [hp:0200037] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skin vesicle
in dataset: phenotype

Lung segmentation defects [hp:0006525]
type: SIO_010056
comment: Phenotype [hp:0006525] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lung segmentation defects
in dataset: phenotype

Abnormality of B cell physiology [hp:0005372]
type: SIO_010056
comment: Phenotype [hp:0005372] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of B cell physiology
in dataset: phenotype

Decreased urinary urate [hp:0011935]
type: SIO_010056
comment: Phenotype [hp:0011935] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased urinary urate
in dataset: phenotype

Facial telangiectasia in butterfly midface distribution [hp:0005598]
type: SIO_010056
comment: Phenotype [hp:0005598] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial telangiectasia in butterfly midface distribution
in dataset: phenotype

Long ear [hp:0400004]
type: SIO_010056
comment: Phenotype [hp:0400004] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long ear
in dataset: phenotype

Heat intolerance [hp:0002046]
type: SIO_010056
comment: Phenotype [hp:0002046] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Heat intolerance
in dataset: phenotype

Macular edema [hp:0040049]
type: SIO_010056
comment: Phenotype [hp:0040049] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macular edema
in dataset: phenotype

Large sternal ossification centers [hp:0006642]
type: SIO_010056
comment: Phenotype [hp:0006642] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large sternal ossification centers
in dataset: phenotype

Absent eyebrow [hp:0002223]
type: SIO_010056
comment: Phenotype [hp:0002223] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent eyebrow
in dataset: phenotype

Refractory anemia [hp:0005505]
type: SIO_010056
comment: Phenotype [hp:0005505] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Refractory anemia
in dataset: phenotype

Hypocalcemic seizures [hp:0002199]
type: SIO_010056
comment: Phenotype [hp:0002199] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypocalcemic seizures
in dataset: phenotype

Elevated pulmonary artery pressure [hp:0004890]
type: SIO_010056
comment: Phenotype [hp:0004890] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated pulmonary artery pressure
in dataset: phenotype

Thickened cortex of long bones [hp:0000935]
type: SIO_010056
comment: Phenotype [hp:0000935] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thickened cortex of long bones
in dataset: phenotype

Aplastic/hypoplastic toenail [hp:0010624]
type: SIO_010056
comment: Phenotype [hp:0010624] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplastic/hypoplastic toenail
in dataset: phenotype

Frontolimbic dementia [hp:0002439]
type: SIO_010056
comment: Phenotype [hp:0002439] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontolimbic dementia
in dataset: phenotype

Telangiectasia of the oral mucosa [hp:0007428]
type: SIO_010056
comment: Phenotype [hp:0007428] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Telangiectasia of the oral mucosa
in dataset: phenotype

Genetic anticipation [hp:0003743]
type: SIO_010056
comment: Phenotype [hp:0003743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Genetic anticipation
in dataset: phenotype

Uterine prolapse [hp:0000139]
type: SIO_010056
comment: Phenotype [hp:0000139] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Uterine prolapse
in dataset: phenotype

Radial bowing [hp:0002986]
type: SIO_010056
comment: Phenotype [hp:0002986] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Radial bowing
in dataset: phenotype

Enlarged epiphyses [hp:0010580]
type: SIO_010056
comment: Phenotype [hp:0010580] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged epiphyses
in dataset: phenotype

Horizontal nystagmus [hp:0000666]
type: SIO_010056
comment: Phenotype [hp:0000666] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Horizontal nystagmus
in dataset: phenotype

Small earlobe [hp:0000385]
type: SIO_010056
comment: Phenotype [hp:0000385] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small earlobe
in dataset: phenotype

Brachyturricephaly [hp:0000244]
type: SIO_010056
comment: Phenotype [hp:0000244] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Brachyturricephaly
in dataset: phenotype

Atypical nevi (>5mm with irregular edge and pigmentation) [hp:0001062]
type: SIO_010056
comment: Phenotype [hp:0001062] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atypical nevi (>5mm with irregular edge and pigmentation)
in dataset: phenotype

Fused sternal ossification centers [hp:0006643]
type: SIO_010056
comment: Phenotype [hp:0006643] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fused sternal ossification centers
in dataset: phenotype

Absent fourth finger distal interphalangeal crease [hp:0005780]
type: SIO_010056
comment: Phenotype [hp:0005780] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent fourth finger distal interphalangeal crease
in dataset: phenotype

Short ear [hp:0400005]
type: SIO_010056
comment: Phenotype [hp:0400005] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short ear
in dataset: phenotype

Extramedullary hematopoiesis [hp:0001978]
type: SIO_010056
comment: Phenotype [hp:0001978] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Extramedullary hematopoiesis
in dataset: phenotype

Skin nodule [hp:0200036]
type: SIO_010056
comment: Phenotype [hp:0200036] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skin nodule
in dataset: phenotype

Anterior pituitary hypoplasia [hp:0010627]
type: SIO_010056
comment: Phenotype [hp:0010627] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior pituitary hypoplasia
in dataset: phenotype

Small, conical teeth [hp:0200141]
type: SIO_010056
comment: Phenotype [hp:0200141] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small, conical teeth
in dataset: phenotype

Decreased central vision [hp:0007663]
type: SIO_010056
comment: Phenotype [hp:0007663] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased central vision
in dataset: phenotype

Flexion contracture of toe [hp:0005830]
type: SIO_010056
comment: Phenotype [hp:0005830] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flexion contracture of toe
in dataset: phenotype

Myelopathy [hp:0002196]
type: SIO_010056
comment: Phenotype [hp:0002196] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myelopathy
in dataset: phenotype

Chronic myelogenous leukemia [hp:0005506]
type: SIO_010056
comment: Phenotype [hp:0005506] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic myelogenous leukemia
in dataset: phenotype

Esophageal stricture [hp:0002043]
type: SIO_010056
comment: Phenotype [hp:0002043] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Esophageal stricture
in dataset: phenotype

Abnormality of the posterior cranial fossa [hp:0000932]
type: SIO_010056
comment: Phenotype [hp:0000932] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the posterior cranial fossa
in dataset: phenotype

Vertigo [hp:0002321]
type: SIO_010056
comment: Phenotype [hp:0002321] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vertigo
in dataset: phenotype

Few cafe-au-lait spots [hp:0007429]
type: SIO_010056
comment: Phenotype [hp:0007429] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Few cafe-au-lait spots
in dataset: phenotype

Genetic anticipation with paternal anticipation bias [hp:0003744]
type: SIO_010056
comment: Phenotype [hp:0003744] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Genetic anticipation with paternal anticipation bias
in dataset: phenotype

Anomalous pulmonary venous return [hp:0010772]
type: SIO_010056
comment: Phenotype [hp:0010772] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anomalous pulmonary venous return
in dataset: phenotype

Postaxial polydactyly [hp:0100259]
type: SIO_010056
comment: Phenotype [hp:0100259] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Postaxial polydactyly
in dataset: phenotype

Phthisis bulbi [hp:0000667]
type: SIO_010056
comment: Phenotype [hp:0000667] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Phthisis bulbi
in dataset: phenotype

Hypopigmented fundi [hp:0001487]
type: SIO_010056
comment: Phenotype [hp:0001487] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypopigmented fundi
in dataset: phenotype

Bifid uterus [hp:0000136]
type: SIO_010056
comment: Phenotype [hp:0000136] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid uterus
in dataset: phenotype

Aged leonine appearance [hp:0008509]
type: SIO_010056
comment: Phenotype [hp:0008509] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aged leonine appearance
in dataset: phenotype

Contractures of the large joints [hp:0005781]
type: SIO_010056
comment: Phenotype [hp:0005781] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Contractures of the large joints
in dataset: phenotype

Lymphoid interstitial pneumonia [hp:0006527]
type: SIO_010056
comment: Phenotype [hp:0006527] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lymphoid interstitial pneumonia
in dataset: phenotype

Skin plaque [hp:0200035]
type: SIO_010056
comment: Phenotype [hp:0200035] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skin plaque
in dataset: phenotype

Microscopic hematuria [hp:0002907]
type: SIO_010056
comment: Phenotype [hp:0002907] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microscopic hematuria
in dataset: phenotype

Hypodontia [hp:0000668]
type: SIO_010056
comment: Phenotype [hp:0000668] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypodontia
in dataset: phenotype

Large tarsal bones [hp:0004679]
type: SIO_010056
comment: Phenotype [hp:0004679] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large tarsal bones
in dataset: phenotype

Diaphyseal cortical sclerosis [hp:0005045]
type: SIO_010056
comment: Phenotype [hp:0005045] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diaphyseal cortical sclerosis
in dataset: phenotype

Delayed menarche [hp:0012569]
type: SIO_010056
comment: Phenotype [hp:0012569] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed menarche
in dataset: phenotype

Thoracic dysplasia [hp:0006644]
type: SIO_010056
comment: Phenotype [hp:0006644] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thoracic dysplasia
in dataset: phenotype

Absent axillary hair [hp:0002221]
type: SIO_010056
comment: Phenotype [hp:0002221] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent axillary hair
in dataset: phenotype

Anterior pituitary agenesis [hp:0010626]
type: SIO_010056
comment: Phenotype [hp:0010626] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior pituitary agenesis
in dataset: phenotype

Posterior fossa cyst at the fourth ventricle [hp:0000933]
type: SIO_010056
comment: Phenotype [hp:0000933] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior fossa cyst at the fourth ventricle
in dataset: phenotype

Impaired distal proprioception [hp:0006858]
type: SIO_010056
comment: Phenotype [hp:0006858] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired distal proprioception
in dataset: phenotype

Zollinger-Ellison syndrome [hp:0002044]
type: SIO_010056
comment: Phenotype [hp:0002044] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Zollinger-Ellison syndrome
in dataset: phenotype

Generalized seizures [hp:0002197]
type: SIO_010056
comment: Phenotype [hp:0002197] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized seizures
in dataset: phenotype

Abnormality of periauricular region [hp:0000383]
type: SIO_010056
comment: Phenotype [hp:0000383] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of periauricular region
in dataset: phenotype

Sporadic [hp:0003745]
type: SIO_010056
comment: Phenotype [hp:0003745] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sporadic
in dataset: phenotype

Irregular epiphyses [hp:0010582]
type: SIO_010056
comment: Phenotype [hp:0010582] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular epiphyses
in dataset: phenotype

Broad palm [hp:0001169]
type: SIO_010056
comment: Phenotype [hp:0001169] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad palm
in dataset: phenotype

Parietal bossing [hp:0000242]
type: SIO_010056
comment: Phenotype [hp:0000242] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Parietal bossing
in dataset: phenotype

Axillary pterygia [hp:0001060]
type: SIO_010056
comment: Phenotype [hp:0001060] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Axillary pterygia
in dataset: phenotype

Renotubular dysgenesis [hp:0008660]
type: SIO_010056
comment: Phenotype [hp:0008660] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renotubular dysgenesis
in dataset: phenotype

Hypoplasia of the radius [hp:0002984]
type: SIO_010056
comment: Phenotype [hp:0002984] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the radius
in dataset: phenotype

Glioblastoma [hp:0100843]
type: SIO_010056
comment: Phenotype [hp:0100843] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glioblastoma
in dataset: phenotype

Bilateral ptosis [hp:0001488]
type: SIO_010056
comment: Phenotype [hp:0001488] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral ptosis
in dataset: phenotype

Abnormality of the ovary [hp:0000137]
type: SIO_010056
comment: Phenotype [hp:0000137] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the ovary
in dataset: phenotype

Increased intraocular pressure [hp:0007906]
type: SIO_010056
comment: Phenotype [hp:0007906] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased intraocular pressure
in dataset: phenotype

Inability to walk [hp:0002540]
type: SIO_010056
comment: Phenotype [hp:0002540] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inability to walk
in dataset: phenotype

Micronodular cirrhosis [hp:0001413]
type: SIO_010056
comment: Phenotype [hp:0001413] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Micronodular cirrhosis
in dataset: phenotype

Obsessive-compulsive behavior [hp:0000722]
type: SIO_010056
comment: Phenotype [hp:0000722] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Obsessive-compulsive behavior
in dataset: phenotype

Abnormality of male internal genitalia [hp:0000022]
type: SIO_010056
comment: Phenotype [hp:0000022] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of male internal genitalia
in dataset: phenotype

Stippled chondral calcification [hp:0002764]
type: SIO_010056
comment: Phenotype [hp:0002764] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stippled chondral calcification
in dataset: phenotype

Finger syndactyly [hp:0006101]
type: SIO_010056
comment: Phenotype [hp:0006101] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Finger syndactyly
in dataset: phenotype

Night blindness [hp:0000662]
type: SIO_010056
comment: Phenotype [hp:0000662] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Night blindness
in dataset: phenotype

Focal seizures [hp:0007359]
type: SIO_010056
comment: Phenotype [hp:0007359] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Focal seizures
in dataset: phenotype

Retinitis pigmentosa inversa [hp:0008035]
type: SIO_010056
comment: Phenotype [hp:0008035] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinitis pigmentosa inversa
in dataset: phenotype

Bone pain [hp:0002653]
type: SIO_010056
comment: Phenotype [hp:0002653] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bone pain
in dataset: phenotype

Flat distal femoral epiphysis [hp:0006398]
type: SIO_010056
comment: Phenotype [hp:0006398] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flat distal femoral epiphysis
in dataset: phenotype

Sparse body hair [hp:0002231]
type: SIO_010056
comment: Phenotype [hp:0002231] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sparse body hair
in dataset: phenotype

Inappropriate laughter [hp:0000748]
type: SIO_010056
comment: Phenotype [hp:0000748] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inappropriate laughter
in dataset: phenotype

Recurrent Haemophilus influenzae infections [hp:0005376]
type: SIO_010056
comment: Phenotype [hp:0005376] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent Haemophilus influenzae infections
in dataset: phenotype

Prostate cancer [hp:0012125]
type: SIO_010056
comment: Phenotype [hp:0012125] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prostate cancer
in dataset: phenotype

Hemoglobinuria [hp:0003641]
type: SIO_010056
comment: Phenotype [hp:0003641] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemoglobinuria
in dataset: phenotype

Potter facies [hp:0002009]
type: SIO_010056
comment: Phenotype [hp:0002009] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Potter facies
in dataset: phenotype

Long-segment aganglionic megacolon [hp:0011285]
type: SIO_010056
comment: Phenotype [hp:0011285] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long-segment aganglionic megacolon
in dataset: phenotype

Global glomerulosclerosis [hp:0004737]
type: SIO_010056
comment: Phenotype [hp:0004737] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Global glomerulosclerosis
in dataset: phenotype

Alveolar proteinosis [hp:0006517]
type: SIO_010056
comment: Phenotype [hp:0006517] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Alveolar proteinosis
in dataset: phenotype

Hypertrophic cardiomyopathy [hp:0001639]
type: SIO_010056
comment: Phenotype [hp:0001639] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertrophic cardiomyopathy
in dataset: phenotype

Hyperchylomicronemia [hp:0012238]
type: SIO_010056
comment: Phenotype [hp:0012238] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperchylomicronemia
in dataset: phenotype

Increased urinary thiosulfate [hp:0011943]
type: SIO_010056
comment: Phenotype [hp:0011943] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased urinary thiosulfate
in dataset: phenotype

Acute myeloid leukemia [hp:0004808]
type: SIO_010056
comment: Phenotype [hp:0004808] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute myeloid leukemia
in dataset: phenotype

Microvesicular hepatic steatosis [hp:0001414]
type: SIO_010056
comment: Phenotype [hp:0001414] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microvesicular hepatic steatosis
in dataset: phenotype

Palpebral fissure narrowing on adduction [hp:0000661]
type: SIO_010056
comment: Phenotype [hp:0000661] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palpebral fissure narrowing on adduction
in dataset: phenotype

Megacystis [hp:0000021]
type: SIO_010056
comment: Phenotype [hp:0000021] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Megacystis
in dataset: phenotype

Abnormal tendon morphology [hp:0100261]
type: SIO_010056
comment: Phenotype [hp:0100261] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal tendon morphology
in dataset: phenotype

Posterior plagiocephaly [hp:0011327]
type: SIO_010056
comment: Phenotype [hp:0011327] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior plagiocephaly
in dataset: phenotype

Abnormal spermatogenesis [hp:0008669]
type: SIO_010056
comment: Phenotype [hp:0008669] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal spermatogenesis
in dataset: phenotype

Obstructive sleep apnea [hp:0002870]
type: SIO_010056
comment: Phenotype [hp:0002870] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Obstructive sleep apnea
in dataset: phenotype

Ulnar claw [hp:0001178]
type: SIO_010056
comment: Phenotype [hp:0001178] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ulnar claw
in dataset: phenotype

Multiple epiphyseal dysplasia [hp:0002654]
type: SIO_010056
comment: Phenotype [hp:0002654] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple epiphyseal dysplasia
in dataset: phenotype

Contractures involving the joints of the feet [hp:0008366]
type: SIO_010056
comment: Phenotype [hp:0008366] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Contractures involving the joints of the feet
in dataset: phenotype

Hypomature dental enamel [hp:0011085]
type: SIO_010056
comment: Phenotype [hp:0011085] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypomature dental enamel
in dataset: phenotype

Platyspondyly [hp:0000926]
type: SIO_010056
comment: Phenotype [hp:0000926] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Platyspondyly
in dataset: phenotype

Synostosis of carpal bones [hp:0005048]
type: SIO_010056
comment: Phenotype [hp:0005048] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Synostosis of carpal bones
in dataset: phenotype

Cardiac fibroma [hp:0010617]
type: SIO_010056
comment: Phenotype [hp:0010617] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cardiac fibroma
in dataset: phenotype

Paroxysmal bursts of laughter [hp:0000749]
type: SIO_010056
comment: Phenotype [hp:0000749] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paroxysmal bursts of laughter
in dataset: phenotype

Dagger-shaped pulp calcifications [hp:0006302]
type: SIO_010056
comment: Phenotype [hp:0006302] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dagger-shaped pulp calcifications
in dataset: phenotype

Patchy alopecia [hp:0002232]
type: SIO_010056
comment: Phenotype [hp:0002232] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Patchy alopecia
in dataset: phenotype

Crossed fused renal ectopia [hp:0004736]
type: SIO_010056
comment: Phenotype [hp:0004736] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Crossed fused renal ectopia
in dataset: phenotype

Intermittent episodes of respiratory insufficiency due to muscle weakness [hp:0004889]
type: SIO_010056
comment: Phenotype [hp:0004889] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intermittent episodes of respiratory insufficiency due to muscle weakness
in dataset: phenotype

Deviation of finger [hp:0004097]
type: SIO_010056
comment: Phenotype [hp:0004097] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deviation of finger
in dataset: phenotype

Dense metaphyseal bands [hp:0100959]
type: SIO_010056
comment: Phenotype [hp:0100959] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dense metaphyseal bands
in dataset: phenotype

Type I transferrin isoform profile [hp:0003642]
type: SIO_010056
comment: Phenotype [hp:0003642] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type I transferrin isoform profile
in dataset: phenotype

Severe expressive language delay [hp:0006863]
type: SIO_010056
comment: Phenotype [hp:0006863] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe expressive language delay
in dataset: phenotype

Small vessel vasculitis [hp:0011944]
type: SIO_010056
comment: Phenotype [hp:0011944] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small vessel vasculitis
in dataset: phenotype

Stomach cancer [hp:0012126]
type: SIO_010056
comment: Phenotype [hp:0012126] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stomach cancer
in dataset: phenotype

Atransferrinemia [hp:0012239]
type: SIO_010056
comment: Phenotype [hp:0012239] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atransferrinemia
in dataset: phenotype

Restrictive behavior [hp:0000723]
type: SIO_010056
comment: Phenotype [hp:0000723] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Restrictive behavior
in dataset: phenotype

Elevated 7-dehydrocholesterol [hp:0010569]
type: SIO_010056
comment: Phenotype [hp:0010569] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated 7-dehydrocholesterol
in dataset: phenotype

Multiple exostoses [hp:0002762]
type: SIO_010056
comment: Phenotype [hp:0002762] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple exostoses
in dataset: phenotype

Cone-shaped epiphyses of phalanges 2 to 5 [hp:0006035]
type: SIO_010056
comment: Phenotype [hp:0006035] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cone-shaped epiphyses of phalanges 2 to 5
in dataset: phenotype

Imperforate hymen [hp:0030011]
type: SIO_010056
comment: Phenotype [hp:0030011] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Imperforate hymen
in dataset: phenotype

Synophrys [hp:0000664]
type: SIO_010056
comment: Phenotype [hp:0000664] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Synophrys
in dataset: phenotype

Partial duplication of the distal phalanx of the 3rd finger [hp:0009968]
type: SIO_010056
comment: Phenotype [hp:0009968] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Partial duplication of the distal phalanx of the 3rd finger
in dataset: phenotype

Neonatal alloimmune thrombocytopenia [hp:0004809]
type: SIO_010056
comment: Phenotype [hp:0004809] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neonatal alloimmune thrombocytopenia
in dataset: phenotype

Preaxial hand polydactyly [hp:0001177]
type: SIO_010056
comment: Phenotype [hp:0001177] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Preaxial hand polydactyly
in dataset: phenotype

Olivopontocerebellar atrophy [hp:0002542]
type: SIO_010056
comment: Phenotype [hp:0002542] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Olivopontocerebellar atrophy
in dataset: phenotype

Absent anterior eye chamber [hp:0008037]
type: SIO_010056
comment: Phenotype [hp:0008037] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent anterior eye chamber
in dataset: phenotype

Spondyloepiphyseal dysplasia [hp:0002655]
type: SIO_010056
comment: Phenotype [hp:0002655] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spondyloepiphyseal dysplasia
in dataset: phenotype

Thickened helices [hp:0000391]
type: SIO_010056
comment: Phenotype [hp:0000391] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thickened helices
in dataset: phenotype

Urinary incontinence [hp:0000020]
type: SIO_010056
comment: Phenotype [hp:0000020] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urinary incontinence
in dataset: phenotype

Delusions [hp:0000746]
type: SIO_010056
comment: Phenotype [hp:0000746] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delusions
in dataset: phenotype

Absent extraocular muscles [hp:0007886]
type: SIO_010056
comment: Phenotype [hp:0007886] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent extraocular muscles
in dataset: phenotype

Adult onset [hp:0003581]
type: SIO_010056
comment: Phenotype [hp:0003581] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adult onset
in dataset: phenotype

Abnormality of the vertebral column [hp:0000925]
type: SIO_010056
comment: Phenotype [hp:0000925] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the vertebral column
in dataset: phenotype

Ovarian fibroma [hp:0010618]
type: SIO_010056
comment: Phenotype [hp:0010618] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ovarian fibroma
in dataset: phenotype

Elevated sweat chloride [hp:0012236]
type: SIO_010056
comment: Phenotype [hp:0012236] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated sweat chloride
in dataset: phenotype

Bronchiolitis obliterans organizing pneumonia [hp:0011945]
type: SIO_010056
comment: Phenotype [hp:0011945] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bronchiolitis obliterans organizing pneumonia
in dataset: phenotype

Cellular immunodeficiency [hp:0005374]
type: SIO_010056
comment: Phenotype [hp:0005374] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cellular immunodeficiency
in dataset: phenotype

Abnormality of the myocardium [hp:0001637]
type: SIO_010056
comment: Phenotype [hp:0001637] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the myocardium
in dataset: phenotype

Alveolar cell carcinoma [hp:0006519]
type: SIO_010056
comment: Phenotype [hp:0006519] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Alveolar cell carcinoma
in dataset: phenotype

Sulfite oxidase deficiency [hp:0003643]
type: SIO_010056
comment: Phenotype [hp:0003643] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sulfite oxidase deficiency
in dataset: phenotype

Frontal bossing [hp:0002007]
type: SIO_010056
comment: Phenotype [hp:0002007] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontal bossing
in dataset: phenotype

Hyperkeratosis lenticularis perstans [hp:0007570]
type: SIO_010056
comment: Phenotype [hp:0007570] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperkeratosis lenticularis perstans
in dataset: phenotype

Hydrometrocolpos [hp:0030010]
type: SIO_010056
comment: Phenotype [hp:0030010] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hydrometrocolpos
in dataset: phenotype

Decreased corneal thickness [hp:0100689]
type: SIO_010056
comment: Phenotype [hp:0100689] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased corneal thickness
in dataset: phenotype

Aplasia/Hypoplasia of the eyebrow [hp:0100840]
type: SIO_010056
comment: Phenotype [hp:0100840] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the eyebrow
in dataset: phenotype

Enteroviral hepatitis [hp:0001412]
type: SIO_010056
comment: Phenotype [hp:0001412] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enteroviral hepatitis
in dataset: phenotype

Large hands [hp:0001176]
type: SIO_010056
comment: Phenotype [hp:0001176] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large hands
in dataset: phenotype

Tarsal synostosis [hp:0008368]
type: SIO_010056
comment: Phenotype [hp:0008368] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tarsal synostosis
in dataset: phenotype

Epiphyseal dysplasia [hp:0002656]
type: SIO_010056
comment: Phenotype [hp:0002656] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Epiphyseal dysplasia
in dataset: phenotype

Pansynostosis [hp:0011325]
type: SIO_010056
comment: Phenotype [hp:0011325] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pansynostosis
in dataset: phenotype

Slowed horizontal saccades [hp:0007885]
type: SIO_010056
comment: Phenotype [hp:0007885] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slowed horizontal saccades
in dataset: phenotype

Abnormality of the skeletal system [hp:0000924]
type: SIO_010056
comment: Phenotype [hp:0000924] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the skeletal system
in dataset: phenotype

Type D brachydactyly [hp:0005627]
type: SIO_010056
comment: Phenotype [hp:0005627] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type D brachydactyly
in dataset: phenotype

Generalized hirsutism [hp:0002230]
type: SIO_010056
comment: Phenotype [hp:0002230] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized hirsutism
in dataset: phenotype

Fibroma of the breast [hp:0010619]
type: SIO_010056
comment: Phenotype [hp:0010619] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fibroma of the breast
in dataset: phenotype

Abnormal iris vasculature [hp:0007905]
type: SIO_010056
comment: Phenotype [hp:0007905] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal iris vasculature
in dataset: phenotype

Psychotic episodes [hp:0000725]
type: SIO_010056
comment: Phenotype [hp:0000725] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Psychotic episodes
in dataset: phenotype

Respiratory failure requiring assisted ventilation [hp:0004887]
type: SIO_010056
comment: Phenotype [hp:0004887] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Respiratory failure requiring assisted ventilation
in dataset: phenotype

Urocanic aciduria [hp:0012237]
type: SIO_010056
comment: Phenotype [hp:0012237] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urocanic aciduria
in dataset: phenotype

Foot polydactyly [hp:0001829]
type: SIO_010056
comment: Phenotype [hp:0001829] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Foot polydactyly
in dataset: phenotype

Cardiomyopathy [hp:0001638]
type: SIO_010056
comment: Phenotype [hp:0001638] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cardiomyopathy
in dataset: phenotype

Crowded carpal bones [hp:0006180]
type: SIO_010056
comment: Phenotype [hp:0006180] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Crowded carpal bones
in dataset: phenotype

Pulmonary venoocclusive disease [hp:0006518]
type: SIO_010056
comment: Phenotype [hp:0006518] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary venoocclusive disease
in dataset: phenotype

Renal cortical microcysts [hp:0004734]
type: SIO_010056
comment: Phenotype [hp:0004734] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal cortical microcysts
in dataset: phenotype

Partial cellular immunodeficiency [hp:0005375]
type: SIO_010056
comment: Phenotype [hp:0005375] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Partial cellular immunodeficiency
in dataset: phenotype

Rachitic rosary [hp:0000897]
type: SIO_010056
comment: Phenotype [hp:0000897] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rachitic rosary
in dataset: phenotype

Spondylometaphyseal dysplasia [hp:0002657]
type: SIO_010056
comment: Phenotype [hp:0002657] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spondylometaphyseal dysplasia
in dataset: phenotype

Chronic pancreatitis [hp:0006280]
type: SIO_010056
comment: Phenotype [hp:0006280] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic pancreatitis
in dataset: phenotype

Choroid plexus cyst [hp:0002190]
type: SIO_010056
comment: Phenotype [hp:0002190] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Choroid plexus cyst
in dataset: phenotype

Male hypogonadism [hp:0000026]
type: SIO_010056
comment: Phenotype [hp:0000026] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Male hypogonadism
in dataset: phenotype

Hamartoma [hp:0010566]
type: SIO_010056
comment: Phenotype [hp:0010566] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hamartoma
in dataset: phenotype

Synostosis of joints [hp:0100240]
type: SIO_010056
comment: Phenotype [hp:0100240] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Synostosis of joints
in dataset: phenotype

Congestive heart failure [hp:0001635]
type: SIO_010056
comment: Phenotype [hp:0001635] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congestive heart failure
in dataset: phenotype

Weight loss [hp:0001824]
type: SIO_010056
comment: Phenotype [hp:0001824] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Weight loss
in dataset: phenotype

Insidious onset [hp:0003587]
type: SIO_010056
comment: Phenotype [hp:0003587] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Insidious onset
in dataset: phenotype

Congenital laryngeal stridor [hp:0004886]
type: SIO_010056
comment: Phenotype [hp:0004886] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital laryngeal stridor
in dataset: phenotype

Dementia [hp:0000726]
type: SIO_010056
comment: Phenotype [hp:0000726] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dementia
in dataset: phenotype

Deep longitudinal plantar crease [hp:0004681]
type: SIO_010056
comment: Phenotype [hp:0004681] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deep longitudinal plantar crease
in dataset: phenotype

Limited pronation/supination of forearm [hp:0006394]
type: SIO_010056
comment: Phenotype [hp:0006394] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited pronation/supination of forearm
in dataset: phenotype

Retinal arteritis [hp:0008030]
type: SIO_010056
comment: Phenotype [hp:0008030] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal arteritis
in dataset: phenotype

Marginal corneal dystrophy [hp:0007880]
type: SIO_010056
comment: Phenotype [hp:0007880] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Marginal corneal dystrophy
in dataset: phenotype

Broad long bones [hp:0005622]
type: SIO_010056
comment: Phenotype [hp:0005622] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad long bones
in dataset: phenotype

Midclavicular aplasia [hp:0006638]
type: SIO_010056
comment: Phenotype [hp:0006638] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Midclavicular aplasia
in dataset: phenotype

Panuveitis [hp:0012121]
type: SIO_010056
comment: Phenotype [hp:0012121] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Panuveitis
in dataset: phenotype

Falciform retinal fold [hp:0001493]
type: SIO_010056
comment: Phenotype [hp:0001493] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Falciform retinal fold
in dataset: phenotype

Radial deviation of the 4th finger [hp:0009279]
type: SIO_010056
comment: Phenotype [hp:0009279] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Radial deviation of the 4th finger
in dataset: phenotype

Facial paralysis [hp:0007209]
type: SIO_010056
comment: Phenotype [hp:0007209] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial paralysis
in dataset: phenotype

Lewy bodies [hp:0100315]
type: SIO_010056
comment: Phenotype [hp:0100315] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lewy bodies
in dataset: phenotype

Fusion of midphalangeal joints [hp:0006187]
type: SIO_010056
comment: Phenotype [hp:0006187] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fusion of midphalangeal joints
in dataset: phenotype

CNS hypomyelination [hp:0003429]
type: SIO_010056
comment: Phenotype [hp:0003429] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: CNS hypomyelination
in dataset: phenotype

Functional abnormality of male internal genitalia [hp:0000025]
type: SIO_010056
comment: Phenotype [hp:0000025] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Functional abnormality of male internal genitalia
in dataset: phenotype

Congenital hemolytic anemia [hp:0004804]
type: SIO_010056
comment: Phenotype [hp:0004804] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital hemolytic anemia
in dataset: phenotype

Decreased liver function [hp:0001410]
type: SIO_010056
comment: Phenotype [hp:0001410] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased liver function
in dataset: phenotype

Spotty hypopigmentation [hp:0005590]
type: SIO_010056
comment: Phenotype [hp:0005590] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spotty hypopigmentation
in dataset: phenotype

Clitoral hypertrophy [hp:0008665]
type: SIO_010056
comment: Phenotype [hp:0008665] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Clitoral hypertrophy
in dataset: phenotype

Hyperpigmented streaks [hp:0007572]
type: SIO_010056
comment: Phenotype [hp:0007572] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperpigmented streaks
in dataset: phenotype

Anterior uveitis [hp:0012122]
type: SIO_010056
comment: Phenotype [hp:0012122] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior uveitis
in dataset: phenotype

Facial cleft [hp:0002006]
type: SIO_010056
comment: Phenotype [hp:0002006] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial cleft
in dataset: phenotype

Frontal lobe dementia [hp:0000727]
type: SIO_010056
comment: Phenotype [hp:0000727] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontal lobe dementia
in dataset: phenotype

Tetralogy of Fallot [hp:0001636]
type: SIO_010056
comment: Phenotype [hp:0001636] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tetralogy of Fallot
in dataset: phenotype

Episodic respiratory distress [hp:0004885]
type: SIO_010056
comment: Phenotype [hp:0004885] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic respiratory distress
in dataset: phenotype

Sternal punctate calcifications [hp:0006637]
type: SIO_010056
comment: Phenotype [hp:0006637] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sternal punctate calcifications
in dataset: phenotype

Posterior Y-sutural cataract [hp:0008031]
type: SIO_010056
comment: Phenotype [hp:0008031] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior Y-sutural cataract
in dataset: phenotype

Congenital exotropia [hp:0008033]
type: SIO_010056
comment: Phenotype [hp:0008033] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital exotropia
in dataset: phenotype

Gonadal dysgenesis, male [hp:0008668]
type: SIO_010056
comment: Phenotype [hp:0008668] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gonadal dysgenesis, male
in dataset: phenotype

Fingerpad telangiectases [hp:0006107]
type: SIO_010056
comment: Phenotype [hp:0006107] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fingerpad telangiectases
in dataset: phenotype

Lateral clavicle hook [hp:0000895]
type: SIO_010056
comment: Phenotype [hp:0000895] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lateral clavicle hook
in dataset: phenotype

Axenfeld anomaly [hp:0001492]
type: SIO_010056
comment: Phenotype [hp:0001492] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Axenfeld anomaly
in dataset: phenotype

Lipemia retinalis [hp:0000660]
type: SIO_010056
comment: Phenotype [hp:0000660] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lipemia retinalis
in dataset: phenotype

Hypersplenism [hp:0001971]
type: SIO_010056
comment: Phenotype [hp:0001971] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypersplenism
in dataset: phenotype

Abnormality of the mitral valve [hp:0001633]
type: SIO_010056
comment: Phenotype [hp:0001633] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the mitral valve
in dataset: phenotype

Limb fasciculations [hp:0007289]
type: SIO_010056
comment: Phenotype [hp:0007289] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb fasciculations
in dataset: phenotype

Prostatitis [hp:0000024]
type: SIO_010056
comment: Phenotype [hp:0000024] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prostatitis
in dataset: phenotype

Bifid epiglottis [hp:0010564]
type: SIO_010056
comment: Phenotype [hp:0010564] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid epiglottis
in dataset: phenotype

Sarcoma [hp:0100242]
type: SIO_010056
comment: Phenotype [hp:0100242] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sarcoma
in dataset: phenotype

Relatively short spine [hp:0002766]
type: SIO_010056
comment: Phenotype [hp:0002766] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Relatively short spine
in dataset: phenotype

Anterior wedging of L2 [hp:0011941]
type: SIO_010056
comment: Phenotype [hp:0011941] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior wedging of L2
in dataset: phenotype

Large forehead [hp:0002003]
type: SIO_010056
comment: Phenotype [hp:0002003] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large forehead
in dataset: phenotype

Abnormality of the skull [hp:0000929]
type: SIO_010056
comment: Phenotype [hp:0000929] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the skull
in dataset: phenotype

Impaired ability to form peer relationships [hp:0000728]
type: SIO_010056
comment: Phenotype [hp:0000728] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired ability to form peer relationships
in dataset: phenotype

Increased susceptibility to fractures [hp:0002659]
type: SIO_010056
comment: Phenotype [hp:0002659] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased susceptibility to fractures
in dataset: phenotype

Handgrip myotonia [hp:0012899]
type: SIO_010056
comment: Phenotype [hp:0012899] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Handgrip myotonia
in dataset: phenotype

Heinz body anemia [hp:0005511]
type: SIO_010056
comment: Phenotype [hp:0005511] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Heinz body anemia
in dataset: phenotype

Abnormal iris pigmentation [hp:0008034]
type: SIO_010056
comment: Phenotype [hp:0008034] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal iris pigmentation
in dataset: phenotype

Congenital fibrosis of extraocular muscles [hp:0001491]
type: SIO_010056
comment: Phenotype [hp:0001491] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital fibrosis of extraocular muscles
in dataset: phenotype

Rib exostoses [hp:0000896]
type: SIO_010056
comment: Phenotype [hp:0000896] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rib exostoses
in dataset: phenotype

Distal symphalangism [hp:0100263]
type: SIO_010056
comment: Phenotype [hp:0100263] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal symphalangism
in dataset: phenotype

Mitral valve prolapse [hp:0001634]
type: SIO_010056
comment: Phenotype [hp:0001634] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mitral valve prolapse
in dataset: phenotype

Tubulointerstitial nephritis [hp:0001970]
type: SIO_010056
comment: Phenotype [hp:0001970] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tubulointerstitial nephritis
in dataset: phenotype

Abnormality of the thumb [hp:0001172]
type: SIO_010056
comment: Phenotype [hp:0001172] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the thumb
in dataset: phenotype

Inguinal hernia [hp:0000023]
type: SIO_010056
comment: Phenotype [hp:0000023] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inguinal hernia
in dataset: phenotype

Enlarged proximal interphalangeal joints [hp:0006185]
type: SIO_010056
comment: Phenotype [hp:0006185] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged proximal interphalangeal joints
in dataset: phenotype

Increased urinary sulfite [hp:0011942]
type: SIO_010056
comment: Phenotype [hp:0011942] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased urinary sulfite
in dataset: phenotype

Weakness of long finger extensor muscles [hp:0009077]
type: SIO_010056
comment: Phenotype [hp:0009077] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Weakness of long finger extensor muscles
in dataset: phenotype

Anorexia [hp:0002039]
type: SIO_010056
comment: Phenotype [hp:0002039] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anorexia
in dataset: phenotype

Macrodactyly [hp:0004099]
type: SIO_010056
comment: Phenotype [hp:0004099] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macrodactyly
in dataset: phenotype

Atrophy of alveolar ridges [hp:0006308]
type: SIO_010056
comment: Phenotype [hp:0006308] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atrophy of alveolar ridges
in dataset: phenotype

Decreased palmar creases [hp:0006184]
type: SIO_010056
comment: Phenotype [hp:0006184] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased palmar creases
in dataset: phenotype

Transient erythroblastopenia [hp:0005510]
type: SIO_010056
comment: Phenotype [hp:0005510] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Transient erythroblastopenia
in dataset: phenotype

Talipes valgus [hp:0004684]
type: SIO_010056
comment: Phenotype [hp:0004684] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Talipes valgus
in dataset: phenotype

Autistic behavior [hp:0000729]
type: SIO_010056
comment: Phenotype [hp:0000729] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autistic behavior
in dataset: phenotype

Thenar muscle weakness [hp:0003427]
type: SIO_010056
comment: Phenotype [hp:0003427] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thenar muscle weakness
in dataset: phenotype

Foam cells in visceral organs and CNS [hp:0003640]
type: SIO_010056
comment: Phenotype [hp:0003640] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Foam cells in visceral organs and CNS
in dataset: phenotype

Severe T lymphocytopenia [hp:0005379]
type: SIO_010056
comment: Phenotype [hp:0005379] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe T lymphocytopenia
in dataset: phenotype

Methylmalonic aciduria [hp:0012120]
type: SIO_010056
comment: Phenotype [hp:0012120] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Methylmalonic aciduria
in dataset: phenotype

Late onset [hp:0003584]
type: SIO_010056
comment: Phenotype [hp:0003584] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Late onset
in dataset: phenotype

Lateral displacement of patellae [hp:0006397]
type: SIO_010056
comment: Phenotype [hp:0006397] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lateral displacement of patellae
in dataset: phenotype

Absent ossification of calvaria [hp:0005623]
type: SIO_010056
comment: Phenotype [hp:0005623] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent ossification of calvaria
in dataset: phenotype

Talon cusp [hp:0011087]
type: SIO_010056
comment: Phenotype [hp:0011087] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Talon cusp
in dataset: phenotype

Hypomineralization of enamel [hp:0006285]
type: SIO_010056
comment: Phenotype [hp:0006285] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypomineralization of enamel
in dataset: phenotype

Ganglioneuroblastoma [hp:0006747]
type: SIO_010056
comment: Phenotype [hp:0006747] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ganglioneuroblastoma
in dataset: phenotype

Decreased serum ceruloplasmin [hp:0010837]
type: SIO_010056
comment: Phenotype [hp:0010837] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased serum ceruloplasmin
in dataset: phenotype

Rhegmatogenous retinal detachment [hp:0012230]
type: SIO_010056
comment: Phenotype [hp:0012230] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rhegmatogenous retinal detachment
in dataset: phenotype

First dorsal interossei muscle weakness [hp:0003392]
type: SIO_010056
comment: Phenotype [hp:0003392] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: First dorsal interossei muscle weakness
in dataset: phenotype

Elevated maternal serum alpha-fetoprotein [hp:0005984]
type: SIO_010056
comment: Phenotype [hp:0005984] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated maternal serum alpha-fetoprotein
in dataset: phenotype

Chromosomal breakage induced by crosslinking agents [hp:0003221]
type: SIO_010056
comment: Phenotype [hp:0003221] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chromosomal breakage induced by crosslinking agents
in dataset: phenotype

First dorsal interossei muscle atrophy [hp:0003426]
type: SIO_010056
comment: Phenotype [hp:0003426] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: First dorsal interossei muscle atrophy
in dataset: phenotype

Pulmonary arteriovenous fistulas [hp:0004952]
type: SIO_010056
comment: Phenotype [hp:0004952] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary arteriovenous fistulas
in dataset: phenotype

Overgrowth of external genitalia [hp:0003247]
type: SIO_010056
comment: Phenotype [hp:0003247] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Overgrowth of external genitalia
in dataset: phenotype

Reduction of neutrophil motility [hp:0005400]
type: SIO_010056
comment: Phenotype [hp:0005400] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduction of neutrophil motility
in dataset: phenotype

Nocturnal hypoventilation [hp:0002877]
type: SIO_010056
comment: Phenotype [hp:0002877] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nocturnal hypoventilation
in dataset: phenotype

Areflexia [hp:0001284]
type: SIO_010056
comment: Phenotype [hp:0001284] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Areflexia
in dataset: phenotype

Wide nose [hp:0000445]
type: SIO_010056
comment: Phenotype [hp:0000445] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Wide nose
in dataset: phenotype

Parkinsonism [hp:0001300]
type: SIO_010056
comment: Phenotype [hp:0001300] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Parkinsonism
in dataset: phenotype

Long chain 3 hydroxyacyl coA dehydrogenase deficiency [hp:0100950]
type: SIO_010056
comment: Phenotype [hp:0100950] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long chain 3 hydroxyacyl coA dehydrogenase deficiency
in dataset: phenotype

Leukonychia [hp:0001820]
type: SIO_010056
comment: Phenotype [hp:0001820] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Leukonychia
in dataset: phenotype

Split hand [hp:0001171]
type: SIO_010056
comment: Phenotype [hp:0001171] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Split hand
in dataset: phenotype

Hip dysplasia [hp:0001385]
type: SIO_010056
comment: Phenotype [hp:0001385] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hip dysplasia
in dataset: phenotype

Decreased serum estradiol [hp:0008214]
type: SIO_010056
comment: Phenotype [hp:0008214] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased serum estradiol
in dataset: phenotype

Parkinsonism with favorable response to dopaminergic medication [hp:0002548]
type: SIO_010056
comment: Phenotype [hp:0002548] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Parkinsonism with favorable response to dopaminergic medication
in dataset: phenotype

Hemimegalencephaly [hp:0007206]
type: SIO_010056
comment: Phenotype [hp:0007206] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemimegalencephaly
in dataset: phenotype

Absent phalangeal crease [hp:0006109]
type: SIO_010056
comment: Phenotype [hp:0006109] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent phalangeal crease
in dataset: phenotype

Recurrent aphthous stomatitis [hp:0011107]
type: SIO_010056
comment: Phenotype [hp:0011107] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent aphthous stomatitis
in dataset: phenotype

Anxiety (with pheochromocytoma) [hp:0000740]
type: SIO_010056
comment: Phenotype [hp:0000740] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anxiety (with pheochromocytoma)
in dataset: phenotype

Abnormality of the antitragus [hp:0009896]
type: SIO_010056
comment: Phenotype [hp:0009896] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the antitragus
in dataset: phenotype

Distal lower limb amyotrophy [hp:0008944]
type: SIO_010056
comment: Phenotype [hp:0008944] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal lower limb amyotrophy
in dataset: phenotype

Yellow-brown discoloration of the teeth [hp:0006286]
type: SIO_010056
comment: Phenotype [hp:0006286] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Yellow-brown discoloration of the teeth
in dataset: phenotype

Mildly elevated creatine phosphokinase [hp:0008180]
type: SIO_010056
comment: Phenotype [hp:0008180] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mildly elevated creatine phosphokinase
in dataset: phenotype

Congenital onychodystrophy [hp:0008394]
type: SIO_010056
comment: Phenotype [hp:0008394] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital onychodystrophy
in dataset: phenotype

Thenar muscle atrophy [hp:0003393]
type: SIO_010056
comment: Phenotype [hp:0003393] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thenar muscle atrophy
in dataset: phenotype

Deficit in phonologic short-term memory [hp:0002549]
type: SIO_010056
comment: Phenotype [hp:0002549] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deficit in phonologic short-term memory
in dataset: phenotype

Exudative retinal detachment [hp:0012231]
type: SIO_010056
comment: Phenotype [hp:0012231] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exudative retinal detachment
in dataset: phenotype

Delayed myelination [hp:0012448]
type: SIO_010056
comment: Phenotype [hp:0012448] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed myelination
in dataset: phenotype

Abdominal aortic aneurysm [hp:0004953]
type: SIO_010056
comment: Phenotype [hp:0004953] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abdominal aortic aneurysm
in dataset: phenotype

Inflammatory myopathy [hp:0009071]
type: SIO_010056
comment: Phenotype [hp:0009071] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inflammatory myopathy
in dataset: phenotype

Peroneal muscle weakness [hp:0011727]
type: SIO_010056
comment: Phenotype [hp:0011727] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peroneal muscle weakness
in dataset: phenotype

Gonadal tissue inappropriate for external genitalia or chromosomal sex [hp:0003248]
type: SIO_010056
comment: Phenotype [hp:0003248] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gonadal tissue inappropriate for external genitalia or chromosomal sex
in dataset: phenotype

Enlarged fossa interpeduncularis [hp:0100951]
type: SIO_010056
comment: Phenotype [hp:0100951] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged fossa interpeduncularis
in dataset: phenotype

Bulbar palsy [hp:0001283]
type: SIO_010056
comment: Phenotype [hp:0001283] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bulbar palsy
in dataset: phenotype

Concave nail [hp:0001598]
type: SIO_010056
comment: Phenotype [hp:0001598] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Concave nail
in dataset: phenotype

Lumbar hemivertebrae [hp:0008439]
type: SIO_010056
comment: Phenotype [hp:0008439] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lumbar hemivertebrae
in dataset: phenotype

Respiratory failure [hp:0002878]
type: SIO_010056
comment: Phenotype [hp:0002878] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Respiratory failure
in dataset: phenotype

Testicular atrophy [hp:0000029]
type: SIO_010056
comment: Phenotype [hp:0000029] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Testicular atrophy
in dataset: phenotype

Episcleritis [hp:0100534]
type: SIO_010056
comment: Phenotype [hp:0100534] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episcleritis
in dataset: phenotype

Narrow nasal bridge [hp:0000446]
type: SIO_010056
comment: Phenotype [hp:0000446] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow nasal bridge
in dataset: phenotype

Apathy [hp:0000741]
type: SIO_010056
comment: Phenotype [hp:0000741] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Apathy
in dataset: phenotype

Gonadotropin deficiency [hp:0008213]
type: SIO_010056
comment: Phenotype [hp:0008213] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gonadotropin deficiency
in dataset: phenotype

Stomatitis [hp:0010280]
type: SIO_010056
comment: Phenotype [hp:0010280] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stomatitis
in dataset: phenotype

Abnormality of the hip joint [hp:0001384]
type: SIO_010056
comment: Phenotype [hp:0001384] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the hip joint
in dataset: phenotype

Anterior tibial bowing [hp:0006390]
type: SIO_010056
comment: Phenotype [hp:0006390] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior tibial bowing
in dataset: phenotype

Loss of ability to walk in early childhood [hp:0008945]
type: SIO_010056
comment: Phenotype [hp:0008945] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Loss of ability to walk in early childhood
in dataset: phenotype

Recurrent sinusitis [hp:0011108]
type: SIO_010056
comment: Phenotype [hp:0011108] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent sinusitis
in dataset: phenotype

Abetalipoproteinemia [hp:0008181]
type: SIO_010056
comment: Phenotype [hp:0008181] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abetalipoproteinemia
in dataset: phenotype

Decreased methylcobalamin [hp:0003223]
type: SIO_010056
comment: Phenotype [hp:0003223] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased methylcobalamin
in dataset: phenotype

Descending aortic aneurysm [hp:0004954]
type: SIO_010056
comment: Phenotype [hp:0004954] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Descending aortic aneurysm
in dataset: phenotype

Decreased Achilles reflex [hp:0009072]
type: SIO_010056
comment: Phenotype [hp:0009072] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased Achilles reflex
in dataset: phenotype

Fasciitis [hp:0100537]
type: SIO_010056
comment: Phenotype [hp:0100537] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fasciitis
in dataset: phenotype

Hallux valgus [hp:0001822]
type: SIO_010056
comment: Phenotype [hp:0001822] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hallux valgus
in dataset: phenotype

Exertional dyspnea [hp:0002875]
type: SIO_010056
comment: Phenotype [hp:0002875] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exertional dyspnea
in dataset: phenotype

Aplasia/hypoplasia of the extremities [hp:0009815]
type: SIO_010056
comment: Phenotype [hp:0009815] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/hypoplasia of the extremities
in dataset: phenotype

Cryptorchidism [hp:0000028]
type: SIO_010056
comment: Phenotype [hp:0000028] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cryptorchidism
in dataset: phenotype

Facial palsy secondary to cranial hyperostosis [hp:0007285]
type: SIO_010056
comment: Phenotype [hp:0007285] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial palsy secondary to cranial hyperostosis
in dataset: phenotype

Abnormality of the nail [hp:0001597]
type: SIO_010056
comment: Phenotype [hp:0001597] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the nail
in dataset: phenotype

Pelvic girdle amyotrophy [hp:0008946]
type: SIO_010056
comment: Phenotype [hp:0008946] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pelvic girdle amyotrophy
in dataset: phenotype

Chronic sinusitis [hp:0011109]
type: SIO_010056
comment: Phenotype [hp:0011109] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic sinusitis
in dataset: phenotype

Abnormal cervical curvature [hp:0005905]
type: SIO_010056
comment: Phenotype [hp:0005905] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal cervical curvature
in dataset: phenotype

Overtubulated long bones [hp:0006391]
type: SIO_010056
comment: Phenotype [hp:0006391] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Overtubulated long bones
in dataset: phenotype

Adrenal gland dysgenesis [hp:0008216]
type: SIO_010056
comment: Phenotype [hp:0008216] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenal gland dysgenesis
in dataset: phenotype

Chronic monilial nail infection [hp:0008396]
type: SIO_010056
comment: Phenotype [hp:0008396] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic monilial nail infection
in dataset: phenotype

Irregular myelin loops [hp:0007208]
type: SIO_010056
comment: Phenotype [hp:0007208] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular myelin loops
in dataset: phenotype

Anesthetic-induced rhabdomylosis [hp:0011439]
type: SIO_010056
comment: Phenotype [hp:0011439] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anesthetic-induced rhabdomylosis
in dataset: phenotype

Increased cellular sensitivity to UV light [hp:0003224]
type: SIO_010056
comment: Phenotype [hp:0003224] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased cellular sensitivity to UV light
in dataset: phenotype

Multinodular goiter [hp:0005987]
type: SIO_010056
comment: Phenotype [hp:0005987] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multinodular goiter
in dataset: phenotype

Adrenocortical hypoplasia [hp:0008182]
type: SIO_010056
comment: Phenotype [hp:0008182] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenocortical hypoplasia
in dataset: phenotype

Advanced eruption of teeth [hp:0006288]
type: SIO_010056
comment: Phenotype [hp:0006288] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Advanced eruption of teeth
in dataset: phenotype

Hypoplasia of the calcaneus [hp:0012789]
type: SIO_010056
comment: Phenotype [hp:0012789] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the calcaneus
in dataset: phenotype

Gowers sign [hp:0003391]
type: SIO_010056
comment: Phenotype [hp:0003391] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gowers sign
in dataset: phenotype

Hypoplastic iris stroma [hp:0007990]
type: SIO_010056
comment: Phenotype [hp:0007990] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic iris stroma
in dataset: phenotype

Recurrent candida infections [hp:0005401]
type: SIO_010056
comment: Phenotype [hp:0005401] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent candida infections
in dataset: phenotype

Adrenal pheochromocytoma [hp:0006748]
type: SIO_010056
comment: Phenotype [hp:0006748] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenal pheochromocytoma
in dataset: phenotype

Thoracolumbar kyphoscoliosis [hp:0003423]
type: SIO_010056
comment: Phenotype [hp:0003423] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thoracolumbar kyphoscoliosis
in dataset: phenotype

Prominent scrotal raphe [hp:0003246]
type: SIO_010056
comment: Phenotype [hp:0003246] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent scrotal raphe
in dataset: phenotype

Periventricular leukomalacia [hp:0006970]
type: SIO_010056
comment: Phenotype [hp:0006970] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Periventricular leukomalacia
in dataset: phenotype

Generalized arterial tortuosity [hp:0004955]
type: SIO_010056
comment: Phenotype [hp:0004955] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized arterial tortuosity
in dataset: phenotype

Progressive proximal muscle weakness [hp:0009073]
type: SIO_010056
comment: Phenotype [hp:0009073] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive proximal muscle weakness
in dataset: phenotype

Broad nail [hp:0001821]
type: SIO_010056
comment: Phenotype [hp:0001821] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad nail
in dataset: phenotype

Lower limb undergrowth [hp:0009816]
type: SIO_010056
comment: Phenotype [hp:0009816] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lower limb undergrowth
in dataset: phenotype

Severe failure to thrive [hp:0001525]
type: SIO_010056
comment: Phenotype [hp:0001525] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe failure to thrive
in dataset: phenotype

Tetany [hp:0001281]
type: SIO_010056
comment: Phenotype [hp:0001281] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tetany
in dataset: phenotype

Convex nasal ridge [hp:0000444]
type: SIO_010056
comment: Phenotype [hp:0000444] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Convex nasal ridge
in dataset: phenotype

Azoospermia [hp:0000027]
type: SIO_010056
comment: Phenotype [hp:0000027] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Azoospermia
in dataset: phenotype

Horizontal jerk nystagmus [hp:0007286]
type: SIO_010056
comment: Phenotype [hp:0007286] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Horizontal jerk nystagmus
in dataset: phenotype

Alopecia [hp:0001596]
type: SIO_010056
comment: Phenotype [hp:0001596] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Alopecia
in dataset: phenotype

Episodic tachypnea [hp:0002876]
type: SIO_010056
comment: Phenotype [hp:0002876] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic tachypnea
in dataset: phenotype

Increased density of long bones [hp:0006392]
type: SIO_010056
comment: Phenotype [hp:0006392] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased density of long bones
in dataset: phenotype

Thin lower lip vermilion [hp:0010282]
type: SIO_010056
comment: Phenotype [hp:0010282] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thin lower lip vermilion
in dataset: phenotype

Pterygium [hp:0001059]
type: SIO_010056
comment: Phenotype [hp:0001059] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pterygium
in dataset: phenotype

Infantile muscular hypotonia [hp:0008947]
type: SIO_010056
comment: Phenotype [hp:0008947] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Infantile muscular hypotonia
in dataset: phenotype

Joint hypermobility [hp:0001382]
type: SIO_010056
comment: Phenotype [hp:0001382] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Joint hypermobility
in dataset: phenotype

Sensory axonal neuropathy [hp:0003390]
type: SIO_010056
comment: Phenotype [hp:0003390] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sensory axonal neuropathy
in dataset: phenotype

Photosensitive tonic-clonic seizures [hp:0007207]
type: SIO_010056
comment: Phenotype [hp:0007207] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Photosensitive tonic-clonic seizures
in dataset: phenotype

Distal tapering femur [hp:0006408]
type: SIO_010056
comment: Phenotype [hp:0006408] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal tapering femur
in dataset: phenotype

Premature delivery because of cervical insufficiency or membrane fragility [hp:0005267]
type: SIO_010056
comment: Phenotype [hp:0005267] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature delivery because of cervical insufficiency or membrane fragility
in dataset: phenotype

Vertebral segmentation defect [hp:0003422]
type: SIO_010056
comment: Phenotype [hp:0003422] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vertebral segmentation defect
in dataset: phenotype

Vitreous hemorrhage [hp:0007902]
type: SIO_010056
comment: Phenotype [hp:0007902] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vitreous hemorrhage
in dataset: phenotype

Prolonged partial thromboplastin time [hp:0003645]
type: SIO_010056
comment: Phenotype [hp:0003645] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolonged partial thromboplastin time
in dataset: phenotype

Hypoplastic left atrium [hp:0005156]
type: SIO_010056
comment: Phenotype [hp:0005156] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic left atrium
in dataset: phenotype

Syringomyelia [hp:0003396]
type: SIO_010056
comment: Phenotype [hp:0003396] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Syringomyelia
in dataset: phenotype

Congenital muscular torticollis [hp:0005988]
type: SIO_010056
comment: Phenotype [hp:0005988] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital muscular torticollis
in dataset: phenotype

Aplasia/Hypoplasia of the hallux [hp:0008362]
type: SIO_010056
comment: Phenotype [hp:0008362] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the hallux
in dataset: phenotype

Underdeveloped supraorbital ridges [hp:0009891]
type: SIO_010056
comment: Phenotype [hp:0009891] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Underdeveloped supraorbital ridges
in dataset: phenotype

Social and occupational deterioration [hp:0007086]
type: SIO_010056
comment: Phenotype [hp:0007086] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Social and occupational deterioration
in dataset: phenotype

Malformed lacrimal ducts [hp:0007993]
type: SIO_010056
comment: Phenotype [hp:0007993] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malformed lacrimal ducts
in dataset: phenotype

Low frustration tolerance [hp:0000744]
type: SIO_010056
comment: Phenotype [hp:0000744] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Low frustration tolerance
in dataset: phenotype

Involuntary jerking movements [hp:0007087]
type: SIO_010056
comment: Phenotype [hp:0007087] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Involuntary jerking movements
in dataset: phenotype

Hypoplastic fifth fingernail [hp:0008398]
type: SIO_010056
comment: Phenotype [hp:0008398] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic fifth fingernail
in dataset: phenotype

Anotia [hp:0009892]
type: SIO_010056
comment: Phenotype [hp:0009892] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anotia
in dataset: phenotype

Aplasia of the parotid gland [hp:0009740]
type: SIO_010056
comment: Phenotype [hp:0009740] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the parotid gland
in dataset: phenotype

Aplasia/Hypoplasia of the tarsal bones [hp:0008363]
type: SIO_010056
comment: Phenotype [hp:0008363] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the tarsal bones
in dataset: phenotype

Gait disturbance [hp:0001288]
type: SIO_010056
comment: Phenotype [hp:0001288] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gait disturbance
in dataset: phenotype

Retrocollis [hp:0002544]
type: SIO_010056
comment: Phenotype [hp:0002544] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retrocollis
in dataset: phenotype

Absent/hypoplastic coccyx [hp:0008436]
type: SIO_010056
comment: Phenotype [hp:0008436] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent/hypoplastic coccyx
in dataset: phenotype

Salivary gland neoplasm [hp:0100684]
type: SIO_010056
comment: Phenotype [hp:0100684] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Salivary gland neoplasm
in dataset: phenotype

Open operculum [hp:0100954]
type: SIO_010056
comment: Phenotype [hp:0100954] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Open operculum
in dataset: phenotype

Abnormality of the hair [hp:0001595]
type: SIO_010056
comment: Phenotype [hp:0001595] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the hair
in dataset: phenotype

Torsion dystonia [hp:0001304]
type: SIO_010056
comment: Phenotype [hp:0001304] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Torsion dystonia
in dataset: phenotype

Upper limb phocomelia [hp:0009813]
type: SIO_010056
comment: Phenotype [hp:0009813] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Upper limb phocomelia
in dataset: phenotype

Generalized lymphadenopathy [hp:0008940]
type: SIO_010056
comment: Phenotype [hp:0008940] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized lymphadenopathy
in dataset: phenotype

Spontaneous abortion [hp:0005268]
type: SIO_010056
comment: Phenotype [hp:0005268] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spontaneous abortion
in dataset: phenotype

Irregular distal femoral epiphysis [hp:0006407]
type: SIO_010056
comment: Phenotype [hp:0006407] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregular distal femoral epiphysis
in dataset: phenotype

Bicarbonaturia [hp:0003646]
type: SIO_010056
comment: Phenotype [hp:0003646] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bicarbonaturia
in dataset: phenotype

Short stature [hp:0004322]
type: SIO_010056
comment: Phenotype [hp:0004322] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short stature
in dataset: phenotype

Pigmented paravenous chorioretinal atrophy [hp:0007903]
type: SIO_010056
comment: Phenotype [hp:0007903] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pigmented paravenous chorioretinal atrophy
in dataset: phenotype

Brain atrophy [hp:0012444]
type: SIO_010056
comment: Phenotype [hp:0012444] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Brain atrophy
in dataset: phenotype

Impaired renal uric acid clearance [hp:0004732]
type: SIO_010056
comment: Phenotype [hp:0004732] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired renal uric acid clearance
in dataset: phenotype

Platyspondyly (childhood) [hp:0003421]
type: SIO_010056
comment: Phenotype [hp:0003421] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Platyspondyly (childhood)
in dataset: phenotype

Generalized hypotonia due to defect at the neuromuscular junction [hp:0003397]
type: SIO_010056
comment: Phenotype [hp:0003397] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized hypotonia due to defect at the neuromuscular junction
in dataset: phenotype

Concentric hypertrophic cardiomyopathy [hp:0005157]
type: SIO_010056
comment: Phenotype [hp:0005157] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Concentric hypertrophic cardiomyopathy
in dataset: phenotype

Redundant neck skin [hp:0005989]
type: SIO_010056
comment: Phenotype [hp:0005989] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Redundant neck skin
in dataset: phenotype

Pseudoepiphyses of the 2nd finger [hp:0009495]
type: SIO_010056
comment: Phenotype [hp:0009495] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pseudoepiphyses of the 2nd finger
in dataset: phenotype

Penile hypospadias [hp:0003244]
type: SIO_010056
comment: Phenotype [hp:0003244] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Penile hypospadias
in dataset: phenotype

High anterior hairline [hp:0009890]
type: SIO_010056
comment: Phenotype [hp:0009890] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High anterior hairline
in dataset: phenotype

Patchy demyelination of subcortical white matter [hp:0002545]
type: SIO_010056
comment: Phenotype [hp:0002545] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Patchy demyelination of subcortical white matter
in dataset: phenotype

Absent in utero ossification of vertebral bodies [hp:0008435]
type: SIO_010056
comment: Phenotype [hp:0008435] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent in utero ossification of vertebral bodies
in dataset: phenotype

Meningitis [hp:0001287]
type: SIO_010056
comment: Phenotype [hp:0001287] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Meningitis
in dataset: phenotype

Ligamentous laxity [hp:0001380]
type: SIO_010056
comment: Phenotype [hp:0001380] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ligamentous laxity
in dataset: phenotype

Nephrosclerosis [hp:0009741]
type: SIO_010056
comment: Phenotype [hp:0009741] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nephrosclerosis
in dataset: phenotype

Abnormality of calcium-phosphate metabolism [hp:0100530]
type: SIO_010056
comment: Phenotype [hp:0100530] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of calcium-phosphate metabolism
in dataset: phenotype

Dandy-Walker malformation [hp:0001305]
type: SIO_010056
comment: Phenotype [hp:0001305] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dandy-Walker malformation
in dataset: phenotype

Right ventricular cardiomyopathy [hp:0011663]
type: SIO_010056
comment: Phenotype [hp:0011663] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Right ventricular cardiomyopathy
in dataset: phenotype

Scoliosis [hp:0002650]
type: SIO_010056
comment: Phenotype [hp:0002650] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scoliosis
in dataset: phenotype

Generalized joint laxity [hp:0002761]
type: SIO_010056
comment: Phenotype [hp:0002761] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized joint laxity
in dataset: phenotype

Electron transfer flavoprotein-ubiquinone oxidoreductase defect [hp:0003647]
type: SIO_010056
comment: Phenotype [hp:0003647] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Electron transfer flavoprotein-ubiquinone oxidoreductase defect
in dataset: phenotype

Fibular overgrowth [hp:0003099]
type: SIO_010056
comment: Phenotype [hp:0003099] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fibular overgrowth
in dataset: phenotype

Hypoplastic lacrimal duct [hp:0007900]
type: SIO_010056
comment: Phenotype [hp:0007900] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic lacrimal duct
in dataset: phenotype

Hemihypertrophy [hp:0001528]
type: SIO_010056
comment: Phenotype [hp:0001528] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemihypertrophy
in dataset: phenotype

Shortened QT interval [hp:0012232]
type: SIO_010056
comment: Phenotype [hp:0012232] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shortened QT interval
in dataset: phenotype

Muscle cramps [hp:0003394]
type: SIO_010056
comment: Phenotype [hp:0003394] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscle cramps
in dataset: phenotype

Precocious puberty in males [hp:0008185]
type: SIO_010056
comment: Phenotype [hp:0008185] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Precocious puberty in males
in dataset: phenotype

Pyelonephritis [hp:0012330]
type: SIO_010056
comment: Phenotype [hp:0012330] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pyelonephritis
in dataset: phenotype

External genital hypoplasia [hp:0003241]
type: SIO_010056
comment: Phenotype [hp:0003241] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: External genital hypoplasia
in dataset: phenotype

Decreased body weight [hp:0004325]
type: SIO_010056
comment: Phenotype [hp:0004325] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased body weight
in dataset: phenotype

Abnormality of the elbow [hp:0009811]
type: SIO_010056
comment: Phenotype [hp:0009811] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the elbow
in dataset: phenotype

Spondyloepimetaphyseal dysplasia [hp:0002651]
type: SIO_010056
comment: Phenotype [hp:0002651] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spondyloepimetaphyseal dysplasia
in dataset: phenotype

Incomprehensible speech [hp:0002546]
type: SIO_010056
comment: Phenotype [hp:0002546] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Incomprehensible speech
in dataset: phenotype

Facial-lingual fasciculations [hp:0007089]
type: SIO_010056
comment: Phenotype [hp:0007089] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial-lingual fasciculations
in dataset: phenotype

Self-mutilation [hp:0000742]
type: SIO_010056
comment: Phenotype [hp:0000742] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Self-mutilation
in dataset: phenotype

Diffuse white matter abnormalities [hp:0007204]
type: SIO_010056
comment: Phenotype [hp:0007204] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse white matter abnormalities
in dataset: phenotype

Central apnea [hp:0002871]
type: SIO_010056
comment: Phenotype [hp:0002871] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Central apnea
in dataset: phenotype

Inflammatory abnormality of the eye [hp:0100533]
type: SIO_010056
comment: Phenotype [hp:0100533] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inflammatory abnormality of the eye
in dataset: phenotype

Acute rhabdomyolysis [hp:0008942]
type: SIO_010056
comment: Phenotype [hp:0008942] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute rhabdomyolysis
in dataset: phenotype

Vertebral arch anomaly [hp:0008438]
type: SIO_010056
comment: Phenotype [hp:0008438] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vertebral arch anomaly
in dataset: phenotype

Enthesitis [hp:0100686]
type: SIO_010056
comment: Phenotype [hp:0100686] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enthesitis
in dataset: phenotype

Bronchogenic cyst [hp:0100730]
type: SIO_010056
comment: Phenotype [hp:0100730] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bronchogenic cyst
in dataset: phenotype

Mood swings [hp:0000720]
type: SIO_010056
comment: Phenotype [hp:0000720] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mood swings
in dataset: phenotype

Single ventricle [hp:0001750]
type: SIO_010056
comment: Phenotype [hp:0001750] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Single ventricle
in dataset: phenotype

Pachygyria [hp:0001302]
type: SIO_010056
comment: Phenotype [hp:0001302] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pachygyria
in dataset: phenotype

Developmental stagnation [hp:0007281]
type: SIO_010056
comment: Phenotype [hp:0007281] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Developmental stagnation
in dataset: phenotype

Lacticaciduria [hp:0003648]
type: SIO_010056
comment: Phenotype [hp:0003648] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lacticaciduria
in dataset: phenotype

Intramuscular hematoma [hp:0012233]
type: SIO_010056
comment: Phenotype [hp:0012233] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intramuscular hematoma
in dataset: phenotype

Abnormality of chromosome stability [hp:0003220]
type: SIO_010056
comment: Phenotype [hp:0003220] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of chromosome stability
in dataset: phenotype

Iridescent posterior subcapsular cataract [hp:0007889]
type: SIO_010056
comment: Phenotype [hp:0007889] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Iridescent posterior subcapsular cataract
in dataset: phenotype

Retinal malformation [hp:0007901]
type: SIO_010056
comment: Phenotype [hp:0007901] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal malformation
in dataset: phenotype

High nonceruloplasmin-bound serum copper [hp:0010838]
type: SIO_010056
comment: Phenotype [hp:0010838] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High nonceruloplasmin-bound serum copper
in dataset: phenotype

Peripheral visual field loss [hp:0007994]
type: SIO_010056
comment: Phenotype [hp:0007994] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral visual field loss
in dataset: phenotype

Increased body weight [hp:0004324]
type: SIO_010056
comment: Phenotype [hp:0004324] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased body weight
in dataset: phenotype

Adrenocortical cytomegaly [hp:0008186]
type: SIO_010056
comment: Phenotype [hp:0008186] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenocortical cytomegaly
in dataset: phenotype

Absence of secondary sex characteristics [hp:0008187]
type: SIO_010056
comment: Phenotype [hp:0008187] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of secondary sex characteristics
in dataset: phenotype

Skeletal dysplasia [hp:0002652]
type: SIO_010056
comment: Phenotype [hp:0002652] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skeletal dysplasia
in dataset: phenotype

Abnormality of the calcaneus [hp:0008364]
type: SIO_010056
comment: Phenotype [hp:0008364] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the calcaneus
in dataset: phenotype

Parathyroid agenesis [hp:0008211]
type: SIO_010056
comment: Phenotype [hp:0008211] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Parathyroid agenesis
in dataset: phenotype

Selective tooth agenesis [hp:0001592]
type: SIO_010056
comment: Phenotype [hp:0001592] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Selective tooth agenesis
in dataset: phenotype

Frontal release signs [hp:0000743]
type: SIO_010056
comment: Phenotype [hp:0000743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontal release signs
in dataset: phenotype

Apneic episodes precipitated by illness, fatigue, stress [hp:0002872]
type: SIO_010056
comment: Phenotype [hp:0002872] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Apneic episodes precipitated by illness, fatigue, stress
in dataset: phenotype

Bifid thoracic vertebrae [hp:0008437]
type: SIO_010056
comment: Phenotype [hp:0008437] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid thoracic vertebrae
in dataset: phenotype

Vestibular dysfunction [hp:0001751]
type: SIO_010056
comment: Phenotype [hp:0001751] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vestibular dysfunction
in dataset: phenotype

Abnormality of the salivary glands [hp:0010286]
type: SIO_010056
comment: Phenotype [hp:0010286] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the salivary glands
in dataset: phenotype

Spastic tetraparesis [hp:0001285]
type: SIO_010056
comment: Phenotype [hp:0001285] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spastic tetraparesis
in dataset: phenotype

Lack of spontaneous play [hp:0000721]
type: SIO_010056
comment: Phenotype [hp:0000721] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lack of spontaneous play
in dataset: phenotype

Ankyloblepharon [hp:0009755]
type: SIO_010056
comment: Phenotype [hp:0009755] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ankyloblepharon
in dataset: phenotype

Very long chain fatty acid accumulation [hp:0008167]
type: SIO_010056
comment: Phenotype [hp:0008167] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Very long chain fatty acid accumulation
in dataset: phenotype

Cervical spinal canal stenosis [hp:0008445]
type: SIO_010056
comment: Phenotype [hp:0008445] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cervical spinal canal stenosis
in dataset: phenotype

Hyporeflexia [hp:0001265]
type: SIO_010056
comment: Phenotype [hp:0001265] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyporeflexia
in dataset: phenotype

Alacrima [hp:0000522]
type: SIO_010056
comment: Phenotype [hp:0000522] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Alacrima
in dataset: phenotype

Seborrheic dermatitis [hp:0001051]
type: SIO_010056
comment: Phenotype [hp:0001051] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Seborrheic dermatitis
in dataset: phenotype

Decreased fertility [hp:0000144]
type: SIO_010056
comment: Phenotype [hp:0000144] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased fertility
in dataset: phenotype

Nevus flammeus of the forehead [hp:0007413]
type: SIO_010056
comment: Phenotype [hp:0007413] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nevus flammeus of the forehead
in dataset: phenotype

Cholangitis [hp:0030151]
type: SIO_010056
comment: Phenotype [hp:0030151] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cholangitis
in dataset: phenotype

Gastrointestinal stroma tumor [hp:0100723]
type: SIO_010056
comment: Phenotype [hp:0100723] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gastrointestinal stroma tumor
in dataset: phenotype

Cessation of head growth [hp:0004485]
type: SIO_010056
comment: Phenotype [hp:0004485] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cessation of head growth
in dataset: phenotype

Broad femoral neck [hp:0006429]
type: SIO_010056
comment: Phenotype [hp:0006429] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad femoral neck
in dataset: phenotype

Transitional cell carcinoma of the bladder [hp:0006740]
type: SIO_010056
comment: Phenotype [hp:0006740] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Transitional cell carcinoma of the bladder
in dataset: phenotype

Widely patent sagittal suture [hp:0005476]
type: SIO_010056
comment: Phenotype [hp:0005476] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Widely patent sagittal suture
in dataset: phenotype

High intestinal obstruction [hp:0005250]
type: SIO_010056
comment: Phenotype [hp:0005250] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High intestinal obstruction
in dataset: phenotype

Joint contracture of the 5th finger [hp:0009183]
type: SIO_010056
comment: Phenotype [hp:0009183] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Joint contracture of the 5th finger
in dataset: phenotype

Enlargement of the ankles [hp:0003029]
type: SIO_010056
comment: Phenotype [hp:0003029] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlargement of the ankles
in dataset: phenotype

Fingerprint intracellular accumulation of autofluorescent lipopigment storage material [hp:0003208]
type: SIO_010056
comment: Phenotype [hp:0003208] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fingerprint intracellular accumulation of autofluorescent lipopigment storage material
in dataset: phenotype

Porokeratosis [hp:0200044]
type: SIO_010056
comment: Phenotype [hp:0200044] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Porokeratosis
in dataset: phenotype

Delayed CNS myelination [hp:0002188]
type: SIO_010056
comment: Phenotype [hp:0002188] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed CNS myelination
in dataset: phenotype

Crystalline corneal dystrophy [hp:0007760]
type: SIO_010056
comment: Phenotype [hp:0007760] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Crystalline corneal dystrophy
in dataset: phenotype

Fibrous syngnathia [hp:0009754]
type: SIO_010056
comment: Phenotype [hp:0009754] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fibrous syngnathia
in dataset: phenotype

Aplasia/Hypoplasia of the fibula [hp:0006492]
type: SIO_010056
comment: Phenotype [hp:0006492] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the fibula
in dataset: phenotype

Choreoathetosis [hp:0001266]
type: SIO_010056
comment: Phenotype [hp:0001266] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Choreoathetosis
in dataset: phenotype

Decreased beta-galactosidase activity [hp:0008166]
type: SIO_010056
comment: Phenotype [hp:0008166] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased beta-galactosidase activity
in dataset: phenotype

Neonatal wrinkled skin of hands and feet [hp:0007414]
type: SIO_010056
comment: Phenotype [hp:0007414] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neonatal wrinkled skin of hands and feet
in dataset: phenotype

EEG with burst suppression [hp:0010851]
type: SIO_010056
comment: Phenotype [hp:0010851] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EEG with burst suppression
in dataset: phenotype

Subcapsular cataract [hp:0000523]
type: SIO_010056
comment: Phenotype [hp:0000523] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subcapsular cataract
in dataset: phenotype

Transverse vaginal septum [hp:0000145]
type: SIO_010056
comment: Phenotype [hp:0000145] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Transverse vaginal septum
in dataset: phenotype

Nevus flammeus [hp:0001052]
type: SIO_010056
comment: Phenotype [hp:0001052] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nevus flammeus
in dataset: phenotype

Hypoplastic ischia [hp:0003175]
type: SIO_010056
comment: Phenotype [hp:0003175] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic ischia
in dataset: phenotype

Excessive daytime sleepiness [hp:0002189]
type: SIO_010056
comment: Phenotype [hp:0002189] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Excessive daytime sleepiness
in dataset: phenotype

Linear arrays of macular hyperkeratoses in flexural areas [hp:0007490]
type: SIO_010056
comment: Phenotype [hp:0007490] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Linear arrays of macular hyperkeratoses in flexural areas
in dataset: phenotype

Short 4th metacarpal [hp:0010044]
type: SIO_010056
comment: Phenotype [hp:0010044] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short 4th metacarpal
in dataset: phenotype

Olivopontocerebellar hypoplasia [hp:0006955]
type: SIO_010056
comment: Phenotype [hp:0006955] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Olivopontocerebellar hypoplasia
in dataset: phenotype

Arterial calcification [hp:0003207]
type: SIO_010056
comment: Phenotype [hp:0003207] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arterial calcification
in dataset: phenotype

Verrucae [hp:0200043]
type: SIO_010056
comment: Phenotype [hp:0200043] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Verrucae
in dataset: phenotype

Horizontal sacrum [hp:0003440]
type: SIO_010056
comment: Phenotype [hp:0003440] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Horizontal sacrum
in dataset: phenotype

Enlarged cerebellum [hp:0012081]
type: SIO_010056
comment: Phenotype [hp:0012081] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged cerebellum
in dataset: phenotype

Patchy palmoplantar keratoderma [hp:0005588]
type: SIO_010056
comment: Phenotype [hp:0005588] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Patchy palmoplantar keratoderma
in dataset: phenotype

Pancreatic islet-cell hyperplasia [hp:0004510]
type: SIO_010056
comment: Phenotype [hp:0004510] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pancreatic islet-cell hyperplasia
in dataset: phenotype

Labial pseudohypertrophy [hp:0008739]
type: SIO_010056
comment: Phenotype [hp:0008739] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Labial pseudohypertrophy
in dataset: phenotype

Reduced circulating T-helper cells [hp:0008165]
type: SIO_010056
comment: Phenotype [hp:0008165] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced circulating T-helper cells
in dataset: phenotype

EEG with photoparoxysmal response [hp:0010852]
type: SIO_010056
comment: Phenotype [hp:0010852] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EEG with photoparoxysmal response
in dataset: phenotype

Abnormality of the tibial metaphysis [hp:0006491]
type: SIO_010056
comment: Phenotype [hp:0006491] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the tibial metaphysis
in dataset: phenotype

Spinal deformities [hp:0008443]
type: SIO_010056
comment: Phenotype [hp:0008443] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinal deformities
in dataset: phenotype

Pallidal degeneration [hp:0007132]
type: SIO_010056
comment: Phenotype [hp:0007132] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pallidal degeneration
in dataset: phenotype

Discrete 2 to 5-mm hyper- and hypopigmented macules [hp:0007494]
type: SIO_010056
comment: Phenotype [hp:0007494] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Discrete 2 to 5-mm hyper- and hypopigmented macules
in dataset: phenotype

Metaphyseal dappling [hp:0011860]
type: SIO_010056
comment: Phenotype [hp:0011860] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metaphyseal dappling
in dataset: phenotype

Mediastinal lymphadenopathy [hp:0100721]
type: SIO_010056
comment: Phenotype [hp:0100721] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mediastinal lymphadenopathy
in dataset: phenotype

Hypopigmented skin patches [hp:0001053]
type: SIO_010056
comment: Phenotype [hp:0001053] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypopigmented skin patches
in dataset: phenotype

Intercrural pterygium [hp:0009757]
type: SIO_010056
comment: Phenotype [hp:0009757] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intercrural pterygium
in dataset: phenotype

Proptosis [hp:0000520]
type: SIO_010056
comment: Phenotype [hp:0000520] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proptosis
in dataset: phenotype

Hypoplastic-absent sebaceous glands [hp:0007411]
type: SIO_010056
comment: Phenotype [hp:0007411] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic-absent sebaceous glands
in dataset: phenotype

Cat cry [hp:0200046]
type: SIO_010056
comment: Phenotype [hp:0200046] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cat cry
in dataset: phenotype

Broad foot [hp:0001769]
type: SIO_010056
comment: Phenotype [hp:0001769] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad foot
in dataset: phenotype

Hand muscle weakness [hp:0030237]
type: SIO_010056
comment: Phenotype [hp:0030237] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hand muscle weakness
in dataset: phenotype

Episodes of ventricular tachycardia [hp:0005141]
type: SIO_010056
comment: Phenotype [hp:0005141] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodes of ventricular tachycardia
in dataset: phenotype

Contracture of the proximal interphalangeal joint of the 5th finger [hp:0009185]
type: SIO_010056
comment: Phenotype [hp:0009185] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Contracture of the proximal interphalangeal joint of the 5th finger
in dataset: phenotype

Mesomelia [hp:0003027]
type: SIO_010056
comment: Phenotype [hp:0003027] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mesomelia
in dataset: phenotype

Hyperactive patellar reflex [hp:0007083]
type: SIO_010056
comment: Phenotype [hp:0007083] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperactive patellar reflex
in dataset: phenotype

Short distal phalanx of the 4th finger [hp:0009290]
type: SIO_010056
comment: Phenotype [hp:0009290] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short distal phalanx of the 4th finger
in dataset: phenotype

Prominent frontal sinuses [hp:0005478]
type: SIO_010056
comment: Phenotype [hp:0005478] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent frontal sinuses
in dataset: phenotype

Decreased activity of NADPH oxidase [hp:0003206]
type: SIO_010056
comment: Phenotype [hp:0003206] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased activity of NADPH oxidase
in dataset: phenotype

Cachexia [hp:0004326]
type: SIO_010056
comment: Phenotype [hp:0004326] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cachexia
in dataset: phenotype

Posterior wedging of vertebral bodies [hp:0008444]
type: SIO_010056
comment: Phenotype [hp:0008444] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior wedging of vertebral bodies
in dataset: phenotype

Mental deterioration [hp:0001268]
type: SIO_010056
comment: Phenotype [hp:0001268] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mental deterioration
in dataset: phenotype

Partially duplicated kidney [hp:0008738]
type: SIO_010056
comment: Phenotype [hp:0008738] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Partially duplicated kidney
in dataset: phenotype

Popliteal pterygium [hp:0009756]
type: SIO_010056
comment: Phenotype [hp:0009756] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Popliteal pterygium
in dataset: phenotype

Progressive peripheral neuropathy [hp:0007133]
type: SIO_010056
comment: Phenotype [hp:0007133] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive peripheral neuropathy
in dataset: phenotype

Polycystic ovaries [hp:0000147]
type: SIO_010056
comment: Phenotype [hp:0000147] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polycystic ovaries
in dataset: phenotype

Numerous nevi [hp:0001054]
type: SIO_010056
comment: Phenotype [hp:0001054] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Numerous nevi
in dataset: phenotype

Hypoplasia of the ear cartilage [hp:0100720]
type: SIO_010056
comment: Phenotype [hp:0100720] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the ear cartilage
in dataset: phenotype

Progressive sclerosis of skull base [hp:0005477]
type: SIO_010056
comment: Phenotype [hp:0005477] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive sclerosis of skull base
in dataset: phenotype

Hypoplastic pubic bone [hp:0003173]
type: SIO_010056
comment: Phenotype [hp:0003173] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic pubic bone
in dataset: phenotype

Craniofacial asymmetry [hp:0004484]
type: SIO_010056
comment: Phenotype [hp:0004484] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Craniofacial asymmetry
in dataset: phenotype

Abnormality of the ankles [hp:0003028]
type: SIO_010056
comment: Phenotype [hp:0003028] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the ankles
in dataset: phenotype

Abnormality of the vitreous humor [hp:0004327]
type: SIO_010056
comment: Phenotype [hp:0004327] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the vitreous humor
in dataset: phenotype

Curvilinear intracellular accumulation of autofluorescent lipopigment storage material [hp:0003205]
type: SIO_010056
comment: Phenotype [hp:0003205] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Curvilinear intracellular accumulation of autofluorescent lipopigment storage material
in dataset: phenotype

Cervical myelopathy [hp:0002318]
type: SIO_010056
comment: Phenotype [hp:0002318] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cervical myelopathy
in dataset: phenotype

Dilated third ventricle [hp:0007082]
type: SIO_010056
comment: Phenotype [hp:0007082] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dilated third ventricle
in dataset: phenotype

Decreased circulating cortisol level [hp:0008163]
type: SIO_010056
comment: Phenotype [hp:0008163] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased circulating cortisol level
in dataset: phenotype

Neck pterygia [hp:0009759]
type: SIO_010056
comment: Phenotype [hp:0009759] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neck pterygia
in dataset: phenotype

Joint swelling [hp:0001386]
type: SIO_010056
comment: Phenotype [hp:0001386] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Joint swelling
in dataset: phenotype

Erysipelas [hp:0001055]
type: SIO_010056
comment: Phenotype [hp:0001055] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Erysipelas
in dataset: phenotype

Cupped ear [hp:0000378]
type: SIO_010056
comment: Phenotype [hp:0000378] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cupped ear
in dataset: phenotype

Complete duplication of distal phalanx of the thumb [hp:0009606]
type: SIO_010056
comment: Phenotype [hp:0009606] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Complete duplication of distal phalanx of the thumb
in dataset: phenotype

Hemiparesis [hp:0001269]
type: SIO_010056
comment: Phenotype [hp:0001269] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemiparesis
in dataset: phenotype

Bilateral conductive hearing impairment [hp:0008513]
type: SIO_010056
comment: Phenotype [hp:0008513] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral conductive hearing impairment
in dataset: phenotype

Unsteady gait [hp:0002317]
type: SIO_010056
comment: Phenotype [hp:0002317] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unsteady gait
in dataset: phenotype

Abnormality of the menstrual cycle [hp:0000140]
type: SIO_010056
comment: Phenotype [hp:0000140] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the menstrual cycle
in dataset: phenotype

Interstitial pulmonary disease [hp:0006530]
type: SIO_010056
comment: Phenotype [hp:0006530] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Interstitial pulmonary disease
in dataset: phenotype

Aplasia/Hypoplasia of the patella [hp:0006498]
type: SIO_010056
comment: Phenotype [hp:0006498] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the patella
in dataset: phenotype

Subungual hyperkeratosis [hp:0008392]
type: SIO_010056
comment: Phenotype [hp:0008392] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subungual hyperkeratosis
in dataset: phenotype

Prominent antitragus [hp:0008593]
type: SIO_010056
comment: Phenotype [hp:0008593] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent antitragus
in dataset: phenotype

Metaphyseal irregularity [hp:0003025]
type: SIO_010056
comment: Phenotype [hp:0003025] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metaphyseal irregularity
in dataset: phenotype

Epidermoid cyst [hp:0200040]
type: SIO_010056
comment: Phenotype [hp:0200040] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Epidermoid cyst
in dataset: phenotype

Adrenocortical carcinoma [hp:0006744]
type: SIO_010056
comment: Phenotype [hp:0006744] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenocortical carcinoma
in dataset: phenotype

Abnormal auditory evoked potentials [hp:0006958]
type: SIO_010056
comment: Phenotype [hp:0006958] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal auditory evoked potentials
in dataset: phenotype

Pleuropulmonary blastoma [hp:0100528]
type: SIO_010056
comment: Phenotype [hp:0100528] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pleuropulmonary blastoma
in dataset: phenotype

Histiocytosis [hp:0100727]
type: SIO_010056
comment: Phenotype [hp:0100727] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Histiocytosis
in dataset: phenotype

Decreased retinal pigmentation with dispersion [hp:0007659]
type: SIO_010056
comment: Phenotype [hp:0007659] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased retinal pigmentation with dispersion
in dataset: phenotype

Narrow iliac wings [hp:0002868]
type: SIO_010056
comment: Phenotype [hp:0002868] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow iliac wings
in dataset: phenotype

Rectilinear intracellular accumulation of autofluorescent lipopigment storage material [hp:0003226]
type: SIO_010056
comment: Phenotype [hp:0003226] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rectilinear intracellular accumulation of autofluorescent lipopigment storage material
in dataset: phenotype

Short 3rd metacarpal [hp:0010041]
type: SIO_010056
comment: Phenotype [hp:0010041] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short 3rd metacarpal
in dataset: phenotype

Progressive macrocephaly [hp:0004481]
type: SIO_010056
comment: Phenotype [hp:0004481] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive macrocephaly
in dataset: phenotype

Aniridia [hp:0000526]
type: SIO_010056
comment: Phenotype [hp:0000526] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aniridia
in dataset: phenotype

First degree atrioventricular block [hp:0011705]
type: SIO_010056
comment: Phenotype [hp:0011705] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: First degree atrioventricular block
in dataset: phenotype

Abnormal sternal ossification [hp:0011863]
type: SIO_010056
comment: Phenotype [hp:0011863] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal sternal ossification
in dataset: phenotype

Palmoplantar hyperhidrosis [hp:0007410]
type: SIO_010056
comment: Phenotype [hp:0007410] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palmoplantar hyperhidrosis
in dataset: phenotype

Pyramidal skinfold extending from the base to the top of the nails [hp:0009758]
type: SIO_010056
comment: Phenotype [hp:0009758] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pyramidal skinfold extending from the base to the top of the nails
in dataset: phenotype

Joint stiffness [hp:0001387]
type: SIO_010056
comment: Phenotype [hp:0001387] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Joint stiffness
in dataset: phenotype

Vertebral hyperostosis [hp:0008442]
type: SIO_010056
comment: Phenotype [hp:0008442] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vertebral hyperostosis
in dataset: phenotype

Hypoplasia of penis [hp:0008736]
type: SIO_010056
comment: Phenotype [hp:0008736] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of penis
in dataset: phenotype

Milia [hp:0001056]
type: SIO_010056
comment: Phenotype [hp:0001056] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Milia
in dataset: phenotype

Poor head control [hp:0002421]
type: SIO_010056
comment: Phenotype [hp:0002421] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poor head control
in dataset: phenotype

Amenorrhea [hp:0000141]
type: SIO_010056
comment: Phenotype [hp:0000141] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Amenorrhea
in dataset: phenotype

Dystrophic fingernails [hp:0008391]
type: SIO_010056
comment: Phenotype [hp:0008391] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dystrophic fingernails
in dataset: phenotype

Pleural lymphangiectasia [hp:0006531]
type: SIO_010056
comment: Phenotype [hp:0006531] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pleural lymphangiectasia
in dataset: phenotype

Increased upper to lower segment ratio [hp:0012774]
type: SIO_010056
comment: Phenotype [hp:0012774] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased upper to lower segment ratio
in dataset: phenotype

Protrusio acetabuli [hp:0003179]
type: SIO_010056
comment: Phenotype [hp:0003179] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Protrusio acetabuli
in dataset: phenotype

Short long bone [hp:0003026]
type: SIO_010056
comment: Phenotype [hp:0003026] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short long bone
in dataset: phenotype

Negative nitroblue tetrazolium (NBT) reduction test [hp:0003203]
type: SIO_010056
comment: Phenotype [hp:0003203] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Negative nitroblue tetrazolium (NBT) reduction test
in dataset: phenotype

Kaposi's sarcoma [hp:0100726]
type: SIO_010056
comment: Phenotype [hp:0100726] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Kaposi's sarcoma
in dataset: phenotype

Reduced phenylalanine hydroxylase activity [hp:0005982]
type: SIO_010056
comment: Phenotype [hp:0005982] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced phenylalanine hydroxylase activity
in dataset: phenotype

Relative macrocephaly [hp:0004482]
type: SIO_010056
comment: Phenotype [hp:0004482] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Relative macrocephaly
in dataset: phenotype

Long eyelashes [hp:0000527]
type: SIO_010056
comment: Phenotype [hp:0000527] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long eyelashes
in dataset: phenotype

Reduced factor V activity [hp:0003225]
type: SIO_010056
comment: Phenotype [hp:0003225] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced factor V activity
in dataset: phenotype

Joint laxity [hp:0001388]
type: SIO_010056
comment: Phenotype [hp:0001388] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Joint laxity
in dataset: phenotype

Intrauterine growth retardation [hp:0001511]
type: SIO_010056
comment: Phenotype [hp:0001511] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intrauterine growth retardation
in dataset: phenotype

Thyroid lymphangiectasia [hp:0008229]
type: SIO_010056
comment: Phenotype [hp:0008229] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thyroid lymphangiectasia
in dataset: phenotype

Complete duplication of proximal phalanx of the thumb [hp:0009608]
type: SIO_010056
comment: Phenotype [hp:0009608] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Complete duplication of proximal phalanx of the thumb
in dataset: phenotype

Elevated plasma pyrophosphate [hp:0011864]
type: SIO_010056
comment: Phenotype [hp:0011864] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated plasma pyrophosphate
in dataset: phenotype

Conjunctival telangiectasia [hp:0000524]
type: SIO_010056
comment: Phenotype [hp:0000524] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Conjunctival telangiectasia
in dataset: phenotype

Abnormality of the vagina [hp:0000142]
type: SIO_010056
comment: Phenotype [hp:0000142] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the vagina
in dataset: phenotype

Headache [hp:0002315]
type: SIO_010056
comment: Phenotype [hp:0002315] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Headache
in dataset: phenotype

Aplasia cutis congenita [hp:0001057]
type: SIO_010056
comment: Phenotype [hp:0001057] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia cutis congenita
in dataset: phenotype

Reduced factor VII activity [hp:0008169]
type: SIO_010056
comment: Phenotype [hp:0008169] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced factor VII activity
in dataset: phenotype

Dilation of lateral ventricles [hp:0006956]
type: SIO_010056
comment: Phenotype [hp:0006956] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dilation of lateral ventricles
in dataset: phenotype

Skeletal muscle atrophy [hp:0003202]
type: SIO_010056
comment: Phenotype [hp:0003202] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skeletal muscle atrophy
in dataset: phenotype

Skin ulcer [hp:0200042]
type: SIO_010056
comment: Phenotype [hp:0200042] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skin ulcer
in dataset: phenotype

Recurrent loss of toenails and fingernails [hp:0008390]
type: SIO_010056
comment: Phenotype [hp:0008390] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent loss of toenails and fingernails
in dataset: phenotype

Decreased calvarial ossification [hp:0005474]
type: SIO_010056
comment: Phenotype [hp:0005474] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased calvarial ossification
in dataset: phenotype

Recurrent cutaneous abscess formation [hp:0100838]
type: SIO_010056
comment: Phenotype [hp:0100838] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent cutaneous abscess formation
in dataset: phenotype

Lichenification [hp:0100725]
type: SIO_010056
comment: Phenotype [hp:0100725] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lichenification
in dataset: phenotype

Hypernatremia [hp:0003228]
type: SIO_010056
comment: Phenotype [hp:0003228] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypernatremia
in dataset: phenotype

Bowing of limbs due to multiple fractures [hp:0003023]
type: SIO_010056
comment: Phenotype [hp:0003023] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bowing of limbs due to multiple fractures
in dataset: phenotype

Neoplasm of the lung [hp:0100526]
type: SIO_010056
comment: Phenotype [hp:0100526] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the lung
in dataset: phenotype

Growth delay [hp:0001510]
type: SIO_010056
comment: Phenotype [hp:0001510] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Growth delay
in dataset: phenotype

Rectovaginal fistula [hp:0000143]
type: SIO_010056
comment: Phenotype [hp:0000143] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rectovaginal fistula
in dataset: phenotype

Degeneration of the lateral corticospinal tracts [hp:0002314]
type: SIO_010056
comment: Phenotype [hp:0002314] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Degeneration of the lateral corticospinal tracts
in dataset: phenotype

Proximal upper limb amyotrophy [hp:0008948]
type: SIO_010056
comment: Phenotype [hp:0008948] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal upper limb amyotrophy
in dataset: phenotype

Poor wound healing [hp:0001058]
type: SIO_010056
comment: Phenotype [hp:0001058] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poor wound healing
in dataset: phenotype

C1-C2 vertebral abnormality [hp:0008440]
type: SIO_010056
comment: Phenotype [hp:0008440] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: C1-C2 vertebral abnormality
in dataset: phenotype

Decreased testicular size [hp:0008734]
type: SIO_010056
comment: Phenotype [hp:0008734] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased testicular size
in dataset: phenotype

Embryonal rhabdomyosarcoma [hp:0006743]
type: SIO_010056
comment: Phenotype [hp:0006743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Embryonal rhabdomyosarcoma
in dataset: phenotype

Skin erosion [hp:0200041]
type: SIO_010056
comment: Phenotype [hp:0200041] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skin erosion
in dataset: phenotype

Rhabdomyolysis [hp:0003201]
type: SIO_010056
comment: Phenotype [hp:0003201] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rhabdomyolysis
in dataset: phenotype

Loss of ability to walk [hp:0006957]
type: SIO_010056
comment: Phenotype [hp:0006957] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Loss of ability to walk
in dataset: phenotype

Aplasia/Hypoplasia of the ulna [hp:0006495]
type: SIO_010056
comment: Phenotype [hp:0006495] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the ulna
in dataset: phenotype

Retinal telangiectasia [hp:0007763]
type: SIO_010056
comment: Phenotype [hp:0007763] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal telangiectasia
in dataset: phenotype

Elongated radius [hp:0006424]
type: SIO_010056
comment: Phenotype [hp:0006424] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elongated radius
in dataset: phenotype

Large hyperpigmented retinal spots [hp:0007658]
type: SIO_010056
comment: Phenotype [hp:0007658] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large hyperpigmented retinal spots
in dataset: phenotype

Flared iliac wings [hp:0002869]
type: SIO_010056
comment: Phenotype [hp:0002869] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flared iliac wings
in dataset: phenotype

Squared iliac bones [hp:0003177]
type: SIO_010056
comment: Phenotype [hp:0003177] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Squared iliac bones
in dataset: phenotype

Fusion of middle ear ossicles [hp:0005473]
type: SIO_010056
comment: Phenotype [hp:0005473] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fusion of middle ear ossicles
in dataset: phenotype

Hypercoagulability [hp:0100724]
type: SIO_010056
comment: Phenotype [hp:0100724] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypercoagulability
in dataset: phenotype

Fava bean-induced hemolytic anemia [hp:0004814]
type: SIO_010056
comment: Phenotype [hp:0004814] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fava bean-induced hemolytic anemia
in dataset: phenotype

Rectal prolapse [hp:0002035]
type: SIO_010056
comment: Phenotype [hp:0002035] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rectal prolapse
in dataset: phenotype

Metaphyseal cupping [hp:0003021]
type: SIO_010056
comment: Phenotype [hp:0003021] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metaphyseal cupping
in dataset: phenotype

Central retinal vessel vascular tortuosity [hp:0007768]
type: SIO_010056
comment: Phenotype [hp:0007768] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Central retinal vessel vascular tortuosity
in dataset: phenotype

Bile duct proliferation [hp:0001408]
type: SIO_010056
comment: Phenotype [hp:0001408] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bile duct proliferation
in dataset: phenotype

Malabsorption [hp:0002024]
type: SIO_010056
comment: Phenotype [hp:0002024] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malabsorption
in dataset: phenotype

Mesiodens [hp:0011067]
type: SIO_010056
comment: Phenotype [hp:0011067] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mesiodens
in dataset: phenotype

Eversion of lateral third of lower eyelids [hp:0007655]
type: SIO_010056
comment: Phenotype [hp:0007655] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Eversion of lateral third of lower eyelids
in dataset: phenotype

Aplasia/Hypoplasia of the iris [hp:0008053]
type: SIO_010056
comment: Phenotype [hp:0008053] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the iris
in dataset: phenotype

Psychosis [hp:0000709]
type: SIO_010056
comment: Phenotype [hp:0000709] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Psychosis
in dataset: phenotype

Hypodysplasia of the corpus callosum [hp:0006849]
type: SIO_010056
comment: Phenotype [hp:0006849] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypodysplasia of the corpus callosum
in dataset: phenotype

Testicular neoplasm [hp:0010788]
type: SIO_010056
comment: Phenotype [hp:0010788] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Testicular neoplasm
in dataset: phenotype

Carpal osteolysis [hp:0001495]
type: SIO_010056
comment: Phenotype [hp:0001495] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Carpal osteolysis
in dataset: phenotype

Abnormality of thumb phalanx [hp:0009602]
type: SIO_010056
comment: Phenotype [hp:0009602] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of thumb phalanx
in dataset: phenotype

Spastic paraparesis [hp:0002313]
type: SIO_010056
comment: Phenotype [hp:0002313] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spastic paraparesis
in dataset: phenotype

Abnormal diaphysis morphology [hp:0000940]
type: SIO_010056
comment: Phenotype [hp:0000940] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal diaphysis morphology
in dataset: phenotype

Desmoid tumors [hp:0100245]
type: SIO_010056
comment: Phenotype [hp:0100245] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Desmoid tumors
in dataset: phenotype

Autophagic vacuoles [hp:0003736]
type: SIO_010056
comment: Phenotype [hp:0003736] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autophagic vacuoles
in dataset: phenotype

Hypertonic dehydration [hp:0001986]
type: SIO_010056
comment: Phenotype [hp:0001986] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertonic dehydration
in dataset: phenotype

Lower limb muscle weakness [hp:0007340]
type: SIO_010056
comment: Phenotype [hp:0007340] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lower limb muscle weakness
in dataset: phenotype

Aplasia/Hypoplasia of the sacrum [hp:0008517]
type: SIO_010056
comment: Phenotype [hp:0008517] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the sacrum
in dataset: phenotype

Dysplastic testes [hp:0008733]
type: SIO_010056
comment: Phenotype [hp:0008733] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysplastic testes
in dataset: phenotype

Lip pit [hp:0100267]
type: SIO_010056
comment: Phenotype [hp:0100267] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lip pit
in dataset: phenotype

Mandibular prognathia [hp:0000303]
type: SIO_010056
comment: Phenotype [hp:0000303] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mandibular prognathia
in dataset: phenotype

Behavioral abnormality [hp:0000708]
type: SIO_010056
comment: Phenotype [hp:0000708] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Behavioral abnormality
in dataset: phenotype

Duplication of renal pelvis [hp:0005580]
type: SIO_010056
comment: Phenotype [hp:0005580] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Duplication of renal pelvis
in dataset: phenotype

Hiatus hernia [hp:0002036]
type: SIO_010056
comment: Phenotype [hp:0002036] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hiatus hernia
in dataset: phenotype

Hypoplasia of the ulna [hp:0003022]
type: SIO_010056
comment: Phenotype [hp:0003022] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the ulna
in dataset: phenotype

Arteritis [hp:0012089]
type: SIO_010056
comment: Phenotype [hp:0012089] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arteritis
in dataset: phenotype

Post-transfusion thrombocytopenia [hp:0004813]
type: SIO_010056
comment: Phenotype [hp:0004813] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Post-transfusion thrombocytopenia
in dataset: phenotype

Benign neoplasm of the central nervous system [hp:0100835]
type: SIO_010056
comment: Phenotype [hp:0100835] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Benign neoplasm of the central nervous system
in dataset: phenotype

Hepatic cysts [hp:0001407]
type: SIO_010056
comment: Phenotype [hp:0001407] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatic cysts
in dataset: phenotype

Osteoarthritis [hp:0002758]
type: SIO_010056
comment: Phenotype [hp:0002758] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteoarthritis
in dataset: phenotype

Lacrimal gland aplasia [hp:0007656]
type: SIO_010056
comment: Phenotype [hp:0007656] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lacrimal gland aplasia
in dataset: phenotype

Anal atresia [hp:0002023]
type: SIO_010056
comment: Phenotype [hp:0002023] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anal atresia
in dataset: phenotype

Cerebral edema [hp:0002181]
type: SIO_010056
comment: Phenotype [hp:0002181] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral edema
in dataset: phenotype

Mitochondrial myopathy [hp:0003737]
type: SIO_010056
comment: Phenotype [hp:0003737] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mitochondrial myopathy
in dataset: phenotype

Hypersegmentation of proximal phalanx of third finger [hp:0011929]
type: SIO_010056
comment: Phenotype [hp:0011929] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypersegmentation of proximal phalanx of third finger
in dataset: phenotype

Hypoplastic thumbnail [hp:0012553]
type: SIO_010056
comment: Phenotype [hp:0012553] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic thumbnail
in dataset: phenotype

Clumsiness [hp:0002312]
type: SIO_010056
comment: Phenotype [hp:0002312] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Clumsiness
in dataset: phenotype

Short diaphyses [hp:0000941]
type: SIO_010056
comment: Phenotype [hp:0000941] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short diaphyses
in dataset: phenotype

Aplasia/Hypoplasia of the thumb [hp:0009601]
type: SIO_010056
comment: Phenotype [hp:0009601] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the thumb
in dataset: phenotype

Anarthria [hp:0002425]
type: SIO_010056
comment: Phenotype [hp:0002425] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anarthria
in dataset: phenotype

Dense calvaria [hp:0000250]
type: SIO_010056
comment: Phenotype [hp:0000250] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dense calvaria
in dataset: phenotype

Neurodegeneration [hp:0002180]
type: SIO_010056
comment: Phenotype [hp:0002180] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neurodegeneration
in dataset: phenotype

Osteoma [hp:0100246]
type: SIO_010056
comment: Phenotype [hp:0100246] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteoma
in dataset: phenotype

Abnormality of the vertebral spinous processes [hp:0008516]
type: SIO_010056
comment: Phenotype [hp:0008516] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the vertebral spinous processes
in dataset: phenotype

Autonomic erectile dysfunction [hp:0008652]
type: SIO_010056
comment: Phenotype [hp:0008652] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autonomic erectile dysfunction
in dataset: phenotype

Diffuse swelling of cerebral white matter [hp:0007341]
type: SIO_010056
comment: Phenotype [hp:0007341] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse swelling of cerebral white matter
in dataset: phenotype

Recurrent staphylococcal infections [hp:0007499]
type: SIO_010056
comment: Phenotype [hp:0007499] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent staphylococcal infections
in dataset: phenotype

Hyperammonemia [hp:0001987]
type: SIO_010056
comment: Phenotype [hp:0001987] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperammonemia
in dataset: phenotype

Anophthalmia [hp:0000528]
type: SIO_010056
comment: Phenotype [hp:0000528] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anophthalmia
in dataset: phenotype

Increased number of teeth [hp:0011069]
type: SIO_010056
comment: Phenotype [hp:0011069] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased number of teeth
in dataset: phenotype

Large face [hp:0100729]
type: SIO_010056
comment: Phenotype [hp:0100729] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large face
in dataset: phenotype

Optic disc hypoplasia [hp:0007766]
type: SIO_010056
comment: Phenotype [hp:0007766] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Optic disc hypoplasia
in dataset: phenotype

Tubular basement membrane disintegration [hp:0005583]
type: SIO_010056
comment: Phenotype [hp:0005583] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Tubular basement membrane disintegration
in dataset: phenotype

Inflammation of the large intestine [hp:0002037]
type: SIO_010056
comment: Phenotype [hp:0002037] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inflammation of the large intestine
in dataset: phenotype

Hyperhistidinemia [hp:0010906]
type: SIO_010056
comment: Phenotype [hp:0010906] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperhistidinemia
in dataset: phenotype

Abnormality of the nervous system [hp:0000707]
type: SIO_010056
comment: Phenotype [hp:0000707] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the nervous system
in dataset: phenotype

Cutaneous mastocytosis [hp:0200151]
type: SIO_010056
comment: Phenotype [hp:0200151] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cutaneous mastocytosis
in dataset: phenotype

Glenoid fossa hypoplasia [hp:0006633]
type: SIO_010056
comment: Phenotype [hp:0006633] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Glenoid fossa hypoplasia
in dataset: phenotype

Recurrent pneumonia [hp:0006532]
type: SIO_010056
comment: Phenotype [hp:0006532] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent pneumonia
in dataset: phenotype

Hypoplastic scapulae [hp:0000882]
type: SIO_010056
comment: Phenotype [hp:0000882] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic scapulae
in dataset: phenotype

Elevated levels of phytanic acid [hp:0010571]
type: SIO_010056
comment: Phenotype [hp:0010571] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated levels of phytanic acid
in dataset: phenotype

Incoordination [hp:0002311]
type: SIO_010056
comment: Phenotype [hp:0002311] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Incoordination
in dataset: phenotype

Urinary tract neoplasm [hp:0010786]
type: SIO_010056
comment: Phenotype [hp:0010786] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urinary tract neoplasm
in dataset: phenotype

Postlingual sensorineural hearing impairment [hp:0008596]
type: SIO_010056
comment: Phenotype [hp:0008596] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Postlingual sensorineural hearing impairment
in dataset: phenotype

High pitched voice [hp:0001620]
type: SIO_010056
comment: Phenotype [hp:0001620] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High pitched voice
in dataset: phenotype

Absent microvilli on the surface of peripheral blood lymphocytes [hp:0002971]
type: SIO_010056
comment: Phenotype [hp:0002971] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent microvilli on the surface of peripheral blood lymphocytes
in dataset: phenotype

Incomplete partition of the cochlea type II [hp:0000376]
type: SIO_010056
comment: Phenotype [hp:0000376] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Incomplete partition of the cochlea type II
in dataset: phenotype

Gastrointestinal hemorrhage [hp:0002239]
type: SIO_010056
comment: Phenotype [hp:0002239] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gastrointestinal hemorrhage
in dataset: phenotype

Abnormal platelet function [hp:0011869]
type: SIO_010056
comment: Phenotype [hp:0011869] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal platelet function
in dataset: phenotype

Germ cell neoplasia [hp:0100728]
type: SIO_010056
comment: Phenotype [hp:0100728] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Germ cell neoplasia
in dataset: phenotype

Anal stenosis [hp:0002025]
type: SIO_010056
comment: Phenotype [hp:0002025] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anal stenosis
in dataset: phenotype

Enlargement of the wrists [hp:0003020]
type: SIO_010056
comment: Phenotype [hp:0003020] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlargement of the wrists
in dataset: phenotype

Odontoma [hp:0011068]
type: SIO_010056
comment: Phenotype [hp:0011068] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Odontoma
in dataset: phenotype

Portal hypertension [hp:0001409]
type: SIO_010056
comment: Phenotype [hp:0001409] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Portal hypertension
in dataset: phenotype

Progressive visual loss [hp:0000529]
type: SIO_010056
comment: Phenotype [hp:0000529] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive visual loss
in dataset: phenotype

Unerupted tooth [hp:0000706]
type: SIO_010056
comment: Phenotype [hp:0000706] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unerupted tooth
in dataset: phenotype

Short digit [hp:0011927]
type: SIO_010056
comment: Phenotype [hp:0011927] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short digit
in dataset: phenotype

Protein avoidance [hp:0002038]
type: SIO_010056
comment: Phenotype [hp:0002038] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Protein avoidance
in dataset: phenotype

Increased serum bile acid concentration during pregnancy [hp:0200150]
type: SIO_010056
comment: Phenotype [hp:0200150] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased serum bile acid concentration during pregnancy
in dataset: phenotype

Absent neutrophil specific granules [hp:0012551]
type: SIO_010056
comment: Phenotype [hp:0012551] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent neutrophil specific granules
in dataset: phenotype

Abnormality of the palpebral fissures [hp:0008050]
type: SIO_010056
comment: Phenotype [hp:0008050] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the palpebral fissures
in dataset: phenotype

Dysostosis multiplex [hp:0000943]
type: SIO_010056
comment: Phenotype [hp:0000943] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysostosis multiplex
in dataset: phenotype

Abnormal mitochondrial shape [hp:0012087]
type: SIO_010056
comment: Phenotype [hp:0012087] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal mitochondrial shape
in dataset: phenotype

Retinal striation [hp:0007654]
type: SIO_010056
comment: Phenotype [hp:0007654] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal striation
in dataset: phenotype

Phonophobia [hp:0002183]
type: SIO_010056
comment: Phenotype [hp:0002183] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Phonophobia
in dataset: phenotype

Bronchodysplasia [hp:0006533]
type: SIO_010056
comment: Phenotype [hp:0006533] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bronchodysplasia
in dataset: phenotype

Fibrosarcoma [hp:0100244]
type: SIO_010056
comment: Phenotype [hp:0100244] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fibrosarcoma
in dataset: phenotype

Microcephaly [hp:0000252]
type: SIO_010056
comment: Phenotype [hp:0000252] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microcephaly
in dataset: phenotype

Orofacial dyskinesia [hp:0002310]
type: SIO_010056
comment: Phenotype [hp:0002310] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Orofacial dyskinesia
in dataset: phenotype

Long-tract signs [hp:0002423]
type: SIO_010056
comment: Phenotype [hp:0002423] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long-tract signs
in dataset: phenotype

Triangular shaped middle phalanx of the 3rd finger [hp:0009436]
type: SIO_010056
comment: Phenotype [hp:0009436] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular shaped middle phalanx of the 3rd finger
in dataset: phenotype

Neoplasm of the small intestine [hp:0100833]
type: SIO_010056
comment: Phenotype [hp:0100833] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the small intestine
in dataset: phenotype

Female external genitalia in individual with 46,XY karyotype [hp:0008730]
type: SIO_010056
comment: Phenotype [hp:0008730] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Female external genitalia in individual with 46,XY karyotype
in dataset: phenotype

Paraplegia [hp:0010550]
type: SIO_010056
comment: Phenotype [hp:0010550] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paraplegia
in dataset: phenotype

Carpal bone hypoplasia [hp:0001498]
type: SIO_010056
comment: Phenotype [hp:0001498] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Carpal bone hypoplasia
in dataset: phenotype

Hypoketotic hypoglycemia [hp:0001985]
type: SIO_010056
comment: Phenotype [hp:0001985] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoketotic hypoglycemia
in dataset: phenotype

Abnormality of the pinna [hp:0000377]
type: SIO_010056
comment: Phenotype [hp:0000377] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the pinna
in dataset: phenotype

Genu varum [hp:0002970]
type: SIO_010056
comment: Phenotype [hp:0002970] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Genu varum
in dataset: phenotype

Multiple cafe-au-lait spots [hp:0007565]
type: SIO_010056
comment: Phenotype [hp:0007565] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple cafe-au-lait spots
in dataset: phenotype

Proportionate short stature [hp:0003508]
type: SIO_010056
comment: Phenotype [hp:0003508] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proportionate short stature
in dataset: phenotype

Elevated alkaline phosphatase of bone origin [hp:0010639]
type: SIO_010056
comment: Phenotype [hp:0010639] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated alkaline phosphatase of bone origin
in dataset: phenotype

Gastroesophageal reflux [hp:0002020]
type: SIO_010056
comment: Phenotype [hp:0002020] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gastroesophageal reflux
in dataset: phenotype

Ectropion of lower eyelids [hp:0007651]
type: SIO_010056
comment: Phenotype [hp:0007651] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectropion of lower eyelids
in dataset: phenotype

Short metacarpal [hp:0010049]
type: SIO_010056
comment: Phenotype [hp:0010049] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short metacarpal
in dataset: phenotype

Abnormality of the metaphyses [hp:0000944]
type: SIO_010056
comment: Phenotype [hp:0000944] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the metaphyses
in dataset: phenotype

Pointed chin [hp:0000307]
type: SIO_010056
comment: Phenotype [hp:0000307] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pointed chin
in dataset: phenotype

Recurrent bronchopulmonary infections [hp:0006538]
type: SIO_010056
comment: Phenotype [hp:0006538] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent bronchopulmonary infections
in dataset: phenotype

Short humerus [hp:0005792]
type: SIO_010056
comment: Phenotype [hp:0005792] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short humerus
in dataset: phenotype

Taurodontia [hp:0000679]
type: SIO_010056
comment: Phenotype [hp:0000679] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Taurodontia
in dataset: phenotype

Congenital hypoplastic anemia [hp:0004810]
type: SIO_010056
comment: Phenotype [hp:0004810] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital hypoplastic anemia
in dataset: phenotype

Spotty hyperpigmentation [hp:0005585]
type: SIO_010056
comment: Phenotype [hp:0005585] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spotty hyperpigmentation
in dataset: phenotype

Deuteranomoly [hp:0011520]
type: SIO_010056
comment: Phenotype [hp:0011520] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deuteranomoly
in dataset: phenotype

Abnormality of the forearm [hp:0002973]
type: SIO_010056
comment: Phenotype [hp:0002973] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the forearm
in dataset: phenotype

Hepatocellular necrosis [hp:0001404]
type: SIO_010056
comment: Phenotype [hp:0001404] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatocellular necrosis
in dataset: phenotype

Shortening of all middle phalanges of the fingers [hp:0006110]
type: SIO_010056
comment: Phenotype [hp:0006110] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shortening of all middle phalanges of the fingers
in dataset: phenotype

Progressive microcephaly [hp:0000253]
type: SIO_010056
comment: Phenotype [hp:0000253] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive microcephaly
in dataset: phenotype

Disproportionate short-limb short stature [hp:0008873]
type: SIO_010056
comment: Phenotype [hp:0008873] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Disproportionate short-limb short stature
in dataset: phenotype

Vaginal atresia [hp:0000148]
type: SIO_010056
comment: Phenotype [hp:0000148] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vaginal atresia
in dataset: phenotype

Atrophy/Degeneration involving the spinal cord [hp:0007344]
type: SIO_010056
comment: Phenotype [hp:0007344] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atrophy/Degeneration involving the spinal cord
in dataset: phenotype

Mouches volantes [hp:0100832]
type: SIO_010056
comment: Phenotype [hp:0100832] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mouches volantes
in dataset: phenotype

Uterine neoplasm [hp:0010784]
type: SIO_010056
comment: Phenotype [hp:0010784] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Uterine neoplasm
in dataset: phenotype

Discoid lupus erythematosus [hp:0007417]
type: SIO_010056
comment: Phenotype [hp:0007417] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Discoid lupus erythematosus
in dataset: phenotype

Abnormality of the middle ear [hp:0000370]
type: SIO_010056
comment: Phenotype [hp:0000370] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the middle ear
in dataset: phenotype

Bracket epiphysis of the middle phalanx of the 5th finger [hp:0009204]
type: SIO_010056
comment: Phenotype [hp:0009204] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bracket epiphysis of the middle phalanx of the 5th finger
in dataset: phenotype

Brachydactyly syndrome [hp:0001156]
type: SIO_010056
comment: Phenotype [hp:0001156] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Brachydactyly syndrome
in dataset: phenotype

IgE deficiency [hp:0005479]
type: SIO_010056
comment: Phenotype [hp:0005479] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: IgE deficiency
in dataset: phenotype

EEG with centrotemporal focal spike waves [hp:0012557]
type: SIO_010056
comment: Phenotype [hp:0012557] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EEG with centrotemporal focal spike waves
in dataset: phenotype

Esophageal atresia [hp:0002032]
type: SIO_010056
comment: Phenotype [hp:0002032] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Esophageal atresia
in dataset: phenotype

Distal ulnar hypoplasia [hp:0005033]
type: SIO_010056
comment: Phenotype [hp:0005033] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal ulnar hypoplasia
in dataset: phenotype

Acute encephalopathy [hp:0006846]
type: SIO_010056
comment: Phenotype [hp:0006846] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute encephalopathy
in dataset: phenotype

Neurofibrillary tangles [hp:0002185]
type: SIO_010056
comment: Phenotype [hp:0002185] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neurofibrillary tangles
in dataset: phenotype

Aplasia of metacarpal bones [hp:0010048]
type: SIO_010056
comment: Phenotype [hp:0010048] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of metacarpal bones
in dataset: phenotype

Decreased activity of mitochondrial ATP synthase complex [hp:0011925]
type: SIO_010056
comment: Phenotype [hp:0011925] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased activity of mitochondrial ATP synthase complex
in dataset: phenotype

Bronchial cartilage hypoplasia [hp:0006539]
type: SIO_010056
comment: Phenotype [hp:0006539] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bronchial cartilage hypoplasia
in dataset: phenotype

Abnormal vertebral segmentation and fusion [hp:0005640]
type: SIO_010056
comment: Phenotype [hp:0005640] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal vertebral segmentation and fusion
in dataset: phenotype

Renal cell carcinoma [hp:0005584]
type: SIO_010056
comment: Phenotype [hp:0005584] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal cell carcinoma
in dataset: phenotype

Chondritis of pinna [hp:0200047]
type: SIO_010056
comment: Phenotype [hp:0200047] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chondritis of pinna
in dataset: phenotype

Short fourth metatarsal [hp:0004689]
type: SIO_010056
comment: Phenotype [hp:0004689] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short fourth metatarsal
in dataset: phenotype

Macrovesicular hepatic steatosis [hp:0001403]
type: SIO_010056
comment: Phenotype [hp:0001403] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macrovesicular hepatic steatosis
in dataset: phenotype

Reduced delayed hypersensitivity [hp:0002972]
type: SIO_010056
comment: Phenotype [hp:0002972] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced delayed hypersensitivity
in dataset: phenotype

Prematurely aged appearance [hp:0007495]
type: SIO_010056
comment: Phenotype [hp:0007495] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prematurely aged appearance
in dataset: phenotype

Ovarian gonadoblastoma [hp:0000149]
type: SIO_010056
comment: Phenotype [hp:0000149] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ovarian gonadoblastoma
in dataset: phenotype

Alopecia totalis [hp:0007418]
type: SIO_010056
comment: Phenotype [hp:0007418] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Alopecia totalis
in dataset: phenotype

Acute demyelinating polyneuropathy [hp:0007131]
type: SIO_010056
comment: Phenotype [hp:0007131] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acute demyelinating polyneuropathy
in dataset: phenotype

Long penis [hp:0000040]
type: SIO_010056
comment: Phenotype [hp:0000040] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long penis
in dataset: phenotype

Thigh hypertrophy [hp:0003733]
type: SIO_010056
comment: Phenotype [hp:0003733] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thigh hypertrophy
in dataset: phenotype

Erythema [hp:0010783]
type: SIO_010056
comment: Phenotype [hp:0010783] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Erythema
in dataset: phenotype

Short 5th metacarpal [hp:0010047]
type: SIO_010056
comment: Phenotype [hp:0010047] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short 5th metacarpal
in dataset: phenotype

Hypoplastic ilia [hp:0000946]
type: SIO_010056
comment: Phenotype [hp:0000946] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic ilia
in dataset: phenotype

Apraxia [hp:0002186]
type: SIO_010056
comment: Phenotype [hp:0002186] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Apraxia
in dataset: phenotype

Poor suck [hp:0002033]
type: SIO_010056
comment: Phenotype [hp:0002033] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Poor suck
in dataset: phenotype

Profuse pigmented skin lesions [hp:0005587]
type: SIO_010056
comment: Phenotype [hp:0005587] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Profuse pigmented skin lesions
in dataset: phenotype

Decreased activity of mitochondrial complex III [hp:0011924]
type: SIO_010056
comment: Phenotype [hp:0011924] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased activity of mitochondrial complex III
in dataset: phenotype

Obstructive lung disease [hp:0006536]
type: SIO_010056
comment: Phenotype [hp:0006536] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Obstructive lung disease
in dataset: phenotype

Intrahepatic cholestasis [hp:0001406]
type: SIO_010056
comment: Phenotype [hp:0001406] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intrahepatic cholestasis
in dataset: phenotype

Recurrent hypoglycemia [hp:0001988]
type: SIO_010056
comment: Phenotype [hp:0001988] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent hypoglycemia
in dataset: phenotype

Acrobrachycephaly [hp:0004487]
type: SIO_010056
comment: Phenotype [hp:0004487] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acrobrachycephaly
in dataset: phenotype

Frontal upsweep of hair [hp:0002236]
type: SIO_010056
comment: Phenotype [hp:0002236] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontal upsweep of hair
in dataset: phenotype

Round ear [hp:0100830]
type: SIO_010056
comment: Phenotype [hp:0100830] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Round ear
in dataset: phenotype

Oligodontia [hp:0000677]
type: SIO_010056
comment: Phenotype [hp:0000677] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oligodontia
in dataset: phenotype

Abnormality of the auditory canal [hp:0000372]
type: SIO_010056
comment: Phenotype [hp:0000372] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the auditory canal
in dataset: phenotype

EMG: myotonic runs [hp:0003730]
type: SIO_010056
comment: Phenotype [hp:0003730] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EMG: myotonic runs
in dataset: phenotype

Chordee [hp:0000041]
type: SIO_010056
comment: Phenotype [hp:0000041] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chordee
in dataset: phenotype

Flexion contracture of thumb [hp:0009600]
type: SIO_010056
comment: Phenotype [hp:0009600] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flexion contracture of thumb
in dataset: phenotype

Recurrent singultus [hp:0100247]
type: SIO_010056
comment: Phenotype [hp:0100247] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent singultus
in dataset: phenotype

Schizencephaly [hp:0010636]
type: SIO_010056
comment: Phenotype [hp:0010636] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Schizencephaly
in dataset: phenotype

Intellectual disability, profound [hp:0002187]
type: SIO_010056
comment: Phenotype [hp:0002187] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intellectual disability, profound
in dataset: phenotype

Progressive ophthalmoplegia [hp:0007650]
type: SIO_010056
comment: Phenotype [hp:0007650] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive ophthalmoplegia
in dataset: phenotype

Triangular shaped middle phalanx of the 5th finger [hp:0009182]
type: SIO_010056
comment: Phenotype [hp:0009182] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular shaped middle phalanx of the 5th finger
in dataset: phenotype

Absent patellar reflexes [hp:0006844]
type: SIO_010056
comment: Phenotype [hp:0006844] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent patellar reflexes
in dataset: phenotype

Dumbbell-shaped long bone [hp:0000947]
type: SIO_010056
comment: Phenotype [hp:0000947] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dumbbell-shaped long bone
in dataset: phenotype

Pyloric stenosis [hp:0002021]
type: SIO_010056
comment: Phenotype [hp:0002021] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pyloric stenosis
in dataset: phenotype

Absent nail of hallux [hp:0012555]
type: SIO_010056
comment: Phenotype [hp:0012555] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent nail of hallux
in dataset: phenotype

Fetal akinesia sequence [hp:0001989]
type: SIO_010056
comment: Phenotype [hp:0001989] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fetal akinesia sequence
in dataset: phenotype

Periportal fibrosis [hp:0001405]
type: SIO_010056
comment: Phenotype [hp:0001405] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Periportal fibrosis
in dataset: phenotype

Decreased activity of mitochondrial complex I [hp:0011923]
type: SIO_010056
comment: Phenotype [hp:0011923] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased activity of mitochondrial complex I
in dataset: phenotype

Hyperpigmentation in sun-exposed areas [hp:0005586]
type: SIO_010056
comment: Phenotype [hp:0005586] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperpigmentation in sun-exposed areas
in dataset: phenotype

Susceptibility to chickenpox [hp:0005360]
type: SIO_010056
comment: Phenotype [hp:0005360] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Susceptibility to chickenpox
in dataset: phenotype

Cortical thickening of long bone diaphyses [hp:0005791]
type: SIO_010056
comment: Phenotype [hp:0005791] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cortical thickening of long bone diaphyses
in dataset: phenotype

Pili canaliculi [hp:0002235]
type: SIO_010056
comment: Phenotype [hp:0002235] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pili canaliculi
in dataset: phenotype

Microretrognathia [hp:0000308]
type: SIO_010056
comment: Phenotype [hp:0000308] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microretrognathia
in dataset: phenotype

Radioulnar synostosis [hp:0002974]
type: SIO_010056
comment: Phenotype [hp:0002974] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Radioulnar synostosis
in dataset: phenotype

Feeding difficulties in infancy [hp:0008872]
type: SIO_010056
comment: Phenotype [hp:0008872] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Feeding difficulties in infancy
in dataset: phenotype

Dental crowding [hp:0000678]
type: SIO_010056
comment: Phenotype [hp:0000678] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dental crowding
in dataset: phenotype

Macrocephaly [hp:0000256]
type: SIO_010056
comment: Phenotype [hp:0000256] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macrocephaly
in dataset: phenotype

Limbic malformations [hp:0007343]
type: SIO_010056
comment: Phenotype [hp:0007343] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limbic malformations
in dataset: phenotype

Plethora [hp:0001050]
type: SIO_010056
comment: Phenotype [hp:0001050] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Plethora
in dataset: phenotype

Skin dimples [hp:0010781]
type: SIO_010056
comment: Phenotype [hp:0010781] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Skin dimples
in dataset: phenotype

Decreased pyruvate carboxylase activity [hp:0003209]
type: SIO_010056
comment: Phenotype [hp:0003209] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased pyruvate carboxylase activity
in dataset: phenotype

Motor aphasia [hp:0002427]
type: SIO_010056
comment: Phenotype [hp:0002427] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Motor aphasia
in dataset: phenotype

Generalized seborrheic dermatitis [hp:0007569]
type: SIO_010056
comment: Phenotype [hp:0007569] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized seborrheic dermatitis
in dataset: phenotype

Absent external genitalia [hp:0000042]
type: SIO_010056
comment: Phenotype [hp:0000042] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent external genitalia
in dataset: phenotype

Syndactyly [hp:0001159]
type: SIO_010056
comment: Phenotype [hp:0001159] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Syndactyly
in dataset: phenotype

Hemiballismus [hp:0100248]
type: SIO_010056
comment: Phenotype [hp:0100248] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemiballismus
in dataset: phenotype

Quadriceps muscle weakness [hp:0003731]
type: SIO_010056
comment: Phenotype [hp:0003731] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Quadriceps muscle weakness
in dataset: phenotype

Hypocortisolemia [hp:0008220]
type: SIO_010056
comment: Phenotype [hp:0008220] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypocortisolemia
in dataset: phenotype

Neonatal respiratory distress [hp:0002643]
type: SIO_010056
comment: Phenotype [hp:0002643] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neonatal respiratory distress
in dataset: phenotype

Axial dystonia [hp:0002530]
type: SIO_010056
comment: Phenotype [hp:0002530] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Axial dystonia
in dataset: phenotype

Cupped ribs [hp:0000887]
type: SIO_010056
comment: Phenotype [hp:0000887] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cupped ribs
in dataset: phenotype

Premature skin wrinkling [hp:0100678]
type: SIO_010056
comment: Phenotype [hp:0100678] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature skin wrinkling
in dataset: phenotype

Delayed skeletal maturation [hp:0002750]
type: SIO_010056
comment: Phenotype [hp:0002750] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Delayed skeletal maturation
in dataset: phenotype

Meningeal calcification [hp:0100250]
type: SIO_010056
comment: Phenotype [hp:0100250] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Meningeal calcification
in dataset: phenotype

Emotional lability [hp:0000712]
type: SIO_010056
comment: Phenotype [hp:0000712] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Emotional lability
in dataset: phenotype

Elongated superior cerebellar peduncle [hp:0011933]
type: SIO_010056
comment: Phenotype [hp:0011933] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elongated superior cerebellar peduncle
in dataset: phenotype

Mild short stature [hp:0003502]
type: SIO_010056
comment: Phenotype [hp:0003502] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mild short stature
in dataset: phenotype

Progressive visual field defects [hp:0007987]
type: SIO_010056
comment: Phenotype [hp:0007987] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive visual field defects
in dataset: phenotype

Constipation [hp:0002019]
type: SIO_010056
comment: Phenotype [hp:0002019] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Constipation
in dataset: phenotype

Deep palmar crease [hp:0006191]
type: SIO_010056
comment: Phenotype [hp:0006191] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deep palmar crease
in dataset: phenotype

Circulating immune complexes [hp:0012224]
type: SIO_010056
comment: Phenotype [hp:0012224] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Circulating immune complexes
in dataset: phenotype

Reduced activity of N-acetylglucosaminyltransferase II [hp:0003655]
type: SIO_010056
comment: Phenotype [hp:0003655] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced activity of N-acetylglucosaminyltransferase II
in dataset: phenotype

Almond-shaped palpebral fissure [hp:0007874]
type: SIO_010056
comment: Phenotype [hp:0007874] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Almond-shaped palpebral fissure
in dataset: phenotype

Disinhibition [hp:0000734]
type: SIO_010056
comment: Phenotype [hp:0000734] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Disinhibition
in dataset: phenotype

Radial metaphyseal irregularity [hp:0004019]
type: SIO_010056
comment: Phenotype [hp:0004019] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Radial metaphyseal irregularity
in dataset: phenotype

Infantile onset [hp:0003593]
type: SIO_010056
comment: Phenotype [hp:0003593] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Infantile onset
in dataset: phenotype

Proximal radio-ulnar synostosis [hp:0005037]
type: SIO_010056
comment: Phenotype [hp:0005037] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal radio-ulnar synostosis
in dataset: phenotype

Hyperacusis [hp:0010780]
type: SIO_010056
comment: Phenotype [hp:0010780] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperacusis
in dataset: phenotype

Lower limb peromelia [hp:0009820]
type: SIO_010056
comment: Phenotype [hp:0009820] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lower limb peromelia
in dataset: phenotype

Hypoplasia of the pyramidal tract [hp:0007348]
type: SIO_010056
comment: Phenotype [hp:0007348] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the pyramidal tract
in dataset: phenotype

Epididymitis [hp:0000031]
type: SIO_010056
comment: Phenotype [hp:0000031] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Epididymitis
in dataset: phenotype

Multiple small medullary renal cysts [hp:0008659]
type: SIO_010056
comment: Phenotype [hp:0008659] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple small medullary renal cysts
in dataset: phenotype

Abnormality of pelvic girdle bone morphology [hp:0002644]
type: SIO_010056
comment: Phenotype [hp:0002644] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of pelvic girdle bone morphology
in dataset: phenotype

Distal widening of metacarpals [hp:0006048]
type: SIO_010056
comment: Phenotype [hp:0006048] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal widening of metacarpals
in dataset: phenotype

Hepatic abscesses due to immunodeficiency [hp:0001400]
type: SIO_010056
comment: Phenotype [hp:0001400] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatic abscesses due to immunodeficiency
in dataset: phenotype

Multiple palmar creases [hp:0006114]
type: SIO_010056
comment: Phenotype [hp:0006114] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple palmar creases
in dataset: phenotype

Kyphoscoliosis [hp:0002751]
type: SIO_010056
comment: Phenotype [hp:0002751] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Kyphoscoliosis
in dataset: phenotype

Aplasia/Hypoplasia involving the central nervous system [hp:0002977]
type: SIO_010056
comment: Phenotype [hp:0002977] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia involving the central nervous system
in dataset: phenotype

Ring fibers [hp:0100305]
type: SIO_010056
comment: Phenotype [hp:0100305] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ring fibers
in dataset: phenotype

Macrodontia of permanent maxillary central incisor [hp:0000675]
type: SIO_010056
comment: Phenotype [hp:0000675] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macrodontia of permanent maxillary central incisor
in dataset: phenotype

Partial humoral immunodeficiency [hp:0005363]
type: SIO_010056
comment: Phenotype [hp:0005363] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Partial humoral immunodeficiency
in dataset: phenotype

Decreased beta-glucocerebrosidase protein and activity [hp:0003656]
type: SIO_010056
comment: Phenotype [hp:0003656] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased beta-glucocerebrosidase protein and activity
in dataset: phenotype

Agitation [hp:0000713]
type: SIO_010056
comment: Phenotype [hp:0000713] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Agitation
in dataset: phenotype

Mesenteric artery aneurysm [hp:0011934]
type: SIO_010056
comment: Phenotype [hp:0011934] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mesenteric artery aneurysm
in dataset: phenotype

Irregularly spaced teeth [hp:0006316]
type: SIO_010056
comment: Phenotype [hp:0006316] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irregularly spaced teeth
in dataset: phenotype

Dense deposit disease [hp:0004746]
type: SIO_010056
comment: Phenotype [hp:0004746] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dense deposit disease
in dataset: phenotype

Abnormality of the cardiovascular system [hp:0001626]
type: SIO_010056
comment: Phenotype [hp:0001626] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the cardiovascular system
in dataset: phenotype

Horizontal ribs [hp:0000888]
type: SIO_010056
comment: Phenotype [hp:0000888] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Horizontal ribs
in dataset: phenotype

Abnormality of the intestine [hp:0002242]
type: SIO_010056
comment: Phenotype [hp:0002242] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the intestine
in dataset: phenotype

Abnormally prominent line of Schwalbe [hp:0007873]
type: SIO_010056
comment: Phenotype [hp:0007873] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormally prominent line of Schwalbe
in dataset: phenotype

Limited knee flexion [hp:0006389]
type: SIO_010056
comment: Phenotype [hp:0006389] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited knee flexion
in dataset: phenotype

Narrow nail [hp:0011313]
type: SIO_010056
comment: Phenotype [hp:0011313] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow nail
in dataset: phenotype

Decreased movement range in interphalangeal joints [hp:0006203]
type: SIO_010056
comment: Phenotype [hp:0006203] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased movement range in interphalangeal joints
in dataset: phenotype

Impaired social interactions [hp:0000735]
type: SIO_010056
comment: Phenotype [hp:0000735] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired social interactions
in dataset: phenotype

Prominent supraorbital arches in adult [hp:0004676]
type: SIO_010056
comment: Phenotype [hp:0004676] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent supraorbital arches in adult
in dataset: phenotype

Hyperextensible hand joints [hp:0005639]
type: SIO_010056
comment: Phenotype [hp:0005639] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperextensible hand joints
in dataset: phenotype

Decreased number of large peripheral myelinated nerve fibers [hp:0003387]
type: SIO_010056
comment: Phenotype [hp:0003387] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased number of large peripheral myelinated nerve fibers
in dataset: phenotype

Chronic constipation [hp:0012450]
type: SIO_010056
comment: Phenotype [hp:0012450] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic constipation
in dataset: phenotype

Gustatory lacrimation [hp:0100274]
type: SIO_010056
comment: Phenotype [hp:0100274] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gustatory lacrimation
in dataset: phenotype

Peripheral thrombosis [hp:0002641]
type: SIO_010056
comment: Phenotype [hp:0002641] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral thrombosis
in dataset: phenotype

Stapes ankylosis [hp:0000381]
type: SIO_010056
comment: Phenotype [hp:0000381] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stapes ankylosis
in dataset: phenotype

Abnormality of finger [hp:0001167]
type: SIO_010056
comment: Phenotype [hp:0001167] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of finger
in dataset: phenotype

Increased T3/T4 ratio [hp:0012559]
type: SIO_010056
comment: Phenotype [hp:0012559] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased T3/T4 ratio
in dataset: phenotype

Normocytic hypoplastic anemia [hp:0004819]
type: SIO_010056
comment: Phenotype [hp:0004819] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Normocytic hypoplastic anemia
in dataset: phenotype

Hyperorality [hp:0000710]
type: SIO_010056
comment: Phenotype [hp:0000710] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperorality
in dataset: phenotype

Intrahepatic biliary dysgenesis [hp:0001401]
type: SIO_010056
comment: Phenotype [hp:0001401] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intrahepatic biliary dysgenesis
in dataset: phenotype

Hydrocele testis [hp:0000034]
type: SIO_010056
comment: Phenotype [hp:0000034] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hydrocele testis
in dataset: phenotype

Atrial flutter [hp:0004749]
type: SIO_010056
comment: Phenotype [hp:0004749] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atrial flutter
in dataset: phenotype

Anodontia [hp:0000674]
type: SIO_010056
comment: Phenotype [hp:0000674] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anodontia
in dataset: phenotype

Sparse bone trabeculae [hp:0002752]
type: SIO_010056
comment: Phenotype [hp:0002752] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sparse bone trabeculae
in dataset: phenotype

Abnormality of creatine metabolism [hp:0012113]
type: SIO_010056
comment: Phenotype [hp:0012113] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of creatine metabolism
in dataset: phenotype

Single median maxillary incisor [hp:0006315]
type: SIO_010056
comment: Phenotype [hp:0006315] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Single median maxillary incisor
in dataset: phenotype

Cellular metachromasia [hp:0003653]
type: SIO_010056
comment: Phenotype [hp:0003653] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cellular metachromasia
in dataset: phenotype

Abnormality of cardiac morphology [hp:0001627]
type: SIO_010056
comment: Phenotype [hp:0001627] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of cardiac morphology
in dataset: phenotype

Decreased facial expression [hp:0004673]
type: SIO_010056
comment: Phenotype [hp:0004673] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased facial expression
in dataset: phenotype

Ovarian teratoma [hp:0012226]
type: SIO_010056
comment: Phenotype [hp:0012226] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ovarian teratoma
in dataset: phenotype

Thimble-shaped middle phalanges of hand [hp:0006193]
type: SIO_010056
comment: Phenotype [hp:0006193] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thimble-shaped middle phalanges of hand
in dataset: phenotype

Episodic generalized hypotonia [hp:0006852]
type: SIO_010056
comment: Phenotype [hp:0006852] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic generalized hypotonia
in dataset: phenotype

Easy fatigability [hp:0003388]
type: SIO_010056
comment: Phenotype [hp:0003388] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Easy fatigability
in dataset: phenotype

Shortening of all phalanges of the toes [hp:0005035]
type: SIO_010056
comment: Phenotype [hp:0005035] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shortening of all phalanges of the toes
in dataset: phenotype

Facial palsy [hp:0010628]
type: SIO_010056
comment: Phenotype [hp:0010628] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial palsy
in dataset: phenotype

Osteoporosis [hp:0000939]
type: SIO_010056
comment: Phenotype [hp:0000939] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteoporosis
in dataset: phenotype

Hypoplastic distal radial epiphyses [hp:0006386]
type: SIO_010056
comment: Phenotype [hp:0006386] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic distal radial epiphyses
in dataset: phenotype

Abnormality of digit [hp:0011297]
type: SIO_010056
comment: Phenotype [hp:0011297] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of digit
in dataset: phenotype

Total cataract [hp:0010700]
type: SIO_010056
comment: Phenotype [hp:0010700] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Total cataract
in dataset: phenotype

Retinal arteriolar occlusion [hp:0007985]
type: SIO_010056
comment: Phenotype [hp:0007985] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal arteriolar occlusion
in dataset: phenotype

Choroidal hemangiomata [hp:0007872]
type: SIO_010056
comment: Phenotype [hp:0007872] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Choroidal hemangiomata
in dataset: phenotype

Protein-losing enteropathy [hp:0002243]
type: SIO_010056
comment: Phenotype [hp:0002243] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Protein-losing enteropathy
in dataset: phenotype

Short attention span [hp:0000736]
type: SIO_010056
comment: Phenotype [hp:0000736] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short attention span
in dataset: phenotype

Abnormality of the clavicle [hp:0000889]
type: SIO_010056
comment: Phenotype [hp:0000889] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the clavicle
in dataset: phenotype

Neoplasm of the colon [hp:0100273]
type: SIO_010056
comment: Phenotype [hp:0100273] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the colon
in dataset: phenotype

Arachnodactyly [hp:0001166]
type: SIO_010056
comment: Phenotype [hp:0001166] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arachnodactyly
in dataset: phenotype

Arteriovenous fistulas of celiac and mesenteric vessels [hp:0002642]
type: SIO_010056
comment: Phenotype [hp:0002642] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arteriovenous fistulas of celiac and mesenteric vessels
in dataset: phenotype

Hepatocellular carcinoma [hp:0001402]
type: SIO_010056
comment: Phenotype [hp:0001402] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatocellular carcinoma
in dataset: phenotype

Restlessness [hp:0000711]
type: SIO_010056
comment: Phenotype [hp:0000711] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Restlessness
in dataset: phenotype

Expanded phalanges with widened medullary cavities [hp:0006112]
type: SIO_010056
comment: Phenotype [hp:0006112] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Expanded phalanges with widened medullary cavities
in dataset: phenotype

Thin bony cortex [hp:0002753]
type: SIO_010056
comment: Phenotype [hp:0002753] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thin bony cortex
in dataset: phenotype

Subcortical white matter calcifications [hp:0007346]
type: SIO_010056
comment: Phenotype [hp:0007346] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subcortical white matter calcifications
in dataset: phenotype

Ambiguous genitalia, male [hp:0000033]
type: SIO_010056
comment: Phenotype [hp:0000033] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ambiguous genitalia, male
in dataset: phenotype

Reduced dihydropyrimidine dehydrogenase activity [hp:0003654]
type: SIO_010056
comment: Phenotype [hp:0003654] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced dihydropyrimidine dehydrogenase activity
in dataset: phenotype

Chronic lung disease [hp:0006528]
type: SIO_010056
comment: Phenotype [hp:0006528] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic lung disease
in dataset: phenotype

Bowing of the legs [hp:0002979]
type: SIO_010056
comment: Phenotype [hp:0002979] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bowing of the legs
in dataset: phenotype

Severe B lymphocytopenia [hp:0005365]
type: SIO_010056
comment: Phenotype [hp:0005365] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe B lymphocytopenia
in dataset: phenotype

Endometrial carcinoma [hp:0012114]
type: SIO_010056
comment: Phenotype [hp:0012114] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Endometrial carcinoma
in dataset: phenotype

Abnormality of the small intestine [hp:0002244]
type: SIO_010056
comment: Phenotype [hp:0002244] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the small intestine
in dataset: phenotype

Urethral stricture [hp:0012227]
type: SIO_010056
comment: Phenotype [hp:0012227] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Urethral stricture
in dataset: phenotype

Split foot [hp:0001839]
type: SIO_010056
comment: Phenotype [hp:0001839] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Split foot
in dataset: phenotype

Cerebellar hemisphere hypoplasia [hp:0100307]
type: SIO_010056
comment: Phenotype [hp:0100307] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebellar hemisphere hypoplasia
in dataset: phenotype

Symmetric spinal nerve root neurofibromas [hp:0006851]
type: SIO_010056
comment: Phenotype [hp:0006851] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Symmetric spinal nerve root neurofibromas
in dataset: phenotype

Overlapping fingers [hp:0010557]
type: SIO_010056
comment: Phenotype [hp:0010557] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Overlapping fingers
in dataset: phenotype

Abnormality of dental color [hp:0011073]
type: SIO_010056
comment: Phenotype [hp:0011073] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of dental color
in dataset: phenotype

Osteopenia [hp:0000938]
type: SIO_010056
comment: Phenotype [hp:0000938] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteopenia
in dataset: phenotype

Hypermobility of distal interphalangeal joints [hp:0006201]
type: SIO_010056
comment: Phenotype [hp:0006201] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypermobility of distal interphalangeal joints
in dataset: phenotype

Irritability [hp:0000737]
type: SIO_010056
comment: Phenotype [hp:0000737] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Irritability
in dataset: phenotype

Reduced amplitude of b-wave (ERG) [hp:0007984]
type: SIO_010056
comment: Phenotype [hp:0007984] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced amplitude of b-wave (ERG)
in dataset: phenotype

Cone-shaped epiphysis [hp:0010579]
type: SIO_010056
comment: Phenotype [hp:0010579] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cone-shaped epiphysis
in dataset: phenotype

Impaired thermal sensitivity [hp:0006901]
type: SIO_010056
comment: Phenotype [hp:0006901] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired thermal sensitivity
in dataset: phenotype

Wide distal femoral metaphysis [hp:0006387]
type: SIO_010056
comment: Phenotype [hp:0006387] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Wide distal femoral metaphysis
in dataset: phenotype

Weak voice [hp:0001621]
type: SIO_010056
comment: Phenotype [hp:0001621] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Weak voice
in dataset: phenotype

Hand polydactyly [hp:0001161]
type: SIO_010056
comment: Phenotype [hp:0001161] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hand polydactyly
in dataset: phenotype

Reduced lymphocyte surface expression of CD43 (sialophorin) [hp:0001983]
type: SIO_010056
comment: Phenotype [hp:0001983] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced lymphocyte surface expression of CD43 (sialophorin)
in dataset: phenotype

Incomplete male pseudohermaphroditism [hp:0008656]
type: SIO_010056
comment: Phenotype [hp:0008656] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Incomplete male pseudohermaphroditism
in dataset: phenotype

Abnormality of the penis [hp:0000036]
type: SIO_010056
comment: Phenotype [hp:0000036] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the penis
in dataset: phenotype

Osteomyelitis [hp:0002754]
type: SIO_010056
comment: Phenotype [hp:0002754] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteomyelitis
in dataset: phenotype

Paucity of anterior horn motor neurons [hp:0007277]
type: SIO_010056
comment: Phenotype [hp:0007277] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paucity of anterior horn motor neurons
in dataset: phenotype

Enlarged flash visual evoked potentials [hp:0008045]
type: SIO_010056
comment: Phenotype [hp:0008045] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged flash visual evoked potentials
in dataset: phenotype

Thin ribs [hp:0000883]
type: SIO_010056
comment: Phenotype [hp:0000883] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thin ribs
in dataset: phenotype

Hypoplasia of the lesser trochanter [hp:0008801]
type: SIO_010056
comment: Phenotype [hp:0008801] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the lesser trochanter
in dataset: phenotype

Burkitt lymphoma [hp:0030080]
type: SIO_010056
comment: Phenotype [hp:0030080] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Burkitt lymphoma
in dataset: phenotype

Stenosis of the medullary cavity of the long bones [hp:0100254]
type: SIO_010056
comment: Phenotype [hp:0100254] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stenosis of the medullary cavity of the long bones
in dataset: phenotype

Hypoplastic spleen [hp:0006270]
type: SIO_010056
comment: Phenotype [hp:0006270] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic spleen
in dataset: phenotype

Proximal tapering of metacarpals [hp:0006119]
type: SIO_010056
comment: Phenotype [hp:0006119] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal tapering of metacarpals
in dataset: phenotype

Congenital intracerebral calcification [hp:0006906]
type: SIO_010056
comment: Phenotype [hp:0006906] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital intracerebral calcification
in dataset: phenotype

Bicoronal synostosis [hp:0011318]
type: SIO_010056
comment: Phenotype [hp:0011318] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bicoronal synostosis
in dataset: phenotype

Aortic dissection [hp:0002647]
type: SIO_010056
comment: Phenotype [hp:0002647] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aortic dissection
in dataset: phenotype

Widened distal phalanges [hp:0006200]
type: SIO_010056
comment: Phenotype [hp:0006200] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Widened distal phalanges
in dataset: phenotype

Foam cells [hp:0003651]
type: SIO_010056
comment: Phenotype [hp:0003651] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Foam cells
in dataset: phenotype

Absent sternal ossification [hp:0006628]
type: SIO_010056
comment: Phenotype [hp:0006628] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent sternal ossification
in dataset: phenotype

Hallucinations [hp:0000738]
type: SIO_010056
comment: Phenotype [hp:0000738] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hallucinations
in dataset: phenotype

Club-shaped distal femur [hp:0006384]
type: SIO_010056
comment: Phenotype [hp:0006384] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Club-shaped distal femur
in dataset: phenotype

Abnormality of radial metaphyses [hp:0004015]
type: SIO_010056
comment: Phenotype [hp:0004015] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of radial metaphyses
in dataset: phenotype

Generalized lipodystrophy [hp:0009064]
type: SIO_010056
comment: Phenotype [hp:0009064] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized lipodystrophy
in dataset: phenotype

Hypoplasia of the ventral pons [hp:0006850]
type: SIO_010056
comment: Phenotype [hp:0006850] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the ventral pons
in dataset: phenotype

Dysphagia [hp:0002015]
type: SIO_010056
comment: Phenotype [hp:0002015] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysphagia
in dataset: phenotype

Rocker bottom foot [hp:0001838]
type: SIO_010056
comment: Phenotype [hp:0001838] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rocker bottom foot
in dataset: phenotype

Chronic diarrhea [hp:0002028]
type: SIO_010056
comment: Phenotype [hp:0002028] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic diarrhea
in dataset: phenotype

Depression [hp:0000716]
type: SIO_010056
comment: Phenotype [hp:0000716] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Depression
in dataset: phenotype

Recurrent streptococcus pneumoniae infections [hp:0005366]
type: SIO_010056
comment: Phenotype [hp:0005366] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent streptococcus pneumoniae infections
in dataset: phenotype

Aplasia/Hypoplasia of the fallopian tube [hp:0008655]
type: SIO_010056
comment: Phenotype [hp:0008655] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the fallopian tube
in dataset: phenotype

Abnormality of the testis [hp:0000035]
type: SIO_010056
comment: Phenotype [hp:0000035] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the testis
in dataset: phenotype

Paroxysmal nocturnal hemoglobinuria [hp:0004818]
type: SIO_010056
comment: Phenotype [hp:0004818] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paroxysmal nocturnal hemoglobinuria
in dataset: phenotype

Sea-blue histiocytosis [hp:0001982]
type: SIO_010056
comment: Phenotype [hp:0001982] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sea-blue histiocytosis
in dataset: phenotype

Premature birth [hp:0001622]
type: SIO_010056
comment: Phenotype [hp:0001622] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature birth
in dataset: phenotype

CSF pleocytosis [hp:0012229]
type: SIO_010056
comment: Phenotype [hp:0012229] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: CSF pleocytosis
in dataset: phenotype

Abnormality of the medullary cavity of the long bones [hp:0100253]
type: SIO_010056
comment: Phenotype [hp:0100253] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the medullary cavity of the long bones
in dataset: phenotype

Osteomyelitis due to immunodeficiency [hp:0002755]
type: SIO_010056
comment: Phenotype [hp:0002755] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteomyelitis due to immunodeficiency
in dataset: phenotype

Abnormality of the retinal vasculature [hp:0008046]
type: SIO_010056
comment: Phenotype [hp:0008046] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the retinal vasculature
in dataset: phenotype

Hypoplasia of the femoral head [hp:0008802]
type: SIO_010056
comment: Phenotype [hp:0008802] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the femoral head
in dataset: phenotype

Prominent sternum [hp:0000884]
type: SIO_010056
comment: Phenotype [hp:0000884] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent sternum
in dataset: phenotype

Diffuse cerebellar atrophy [hp:0100275]
type: SIO_010056
comment: Phenotype [hp:0100275] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse cerebellar atrophy
in dataset: phenotype

Shortening of all distal phalanges of the fingers [hp:0006118]
type: SIO_010056
comment: Phenotype [hp:0006118] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shortening of all distal phalanges of the fingers
in dataset: phenotype

Middle age onset [hp:0003596]
type: SIO_010056
comment: Phenotype [hp:0003596] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Middle age onset
in dataset: phenotype

Abnormality of calvarial morphology [hp:0002648]
type: SIO_010056
comment: Phenotype [hp:0002648] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of calvarial morphology
in dataset: phenotype

Short lower limbs [hp:0006385]
type: SIO_010056
comment: Phenotype [hp:0006385] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short lower limbs
in dataset: phenotype

Anxiety [hp:0000739]
type: SIO_010056
comment: Phenotype [hp:0000739] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anxiety
in dataset: phenotype

Abdominal pain [hp:0002027]
type: SIO_010056
comment: Phenotype [hp:0002027] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abdominal pain
in dataset: phenotype

Calcification of the aorta [hp:0004963]
type: SIO_010056
comment: Phenotype [hp:0004963] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcification of the aorta
in dataset: phenotype

Recurrent myoglobinuria [hp:0003652]
type: SIO_010056
comment: Phenotype [hp:0003652] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent myoglobinuria
in dataset: phenotype

Autism [hp:0000717]
type: SIO_010056
comment: Phenotype [hp:0000717] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autism
in dataset: phenotype

Broad toe [hp:0001837]
type: SIO_010056
comment: Phenotype [hp:0001837] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad toe
in dataset: phenotype

Diaphyseal dysplasia [hp:0100252]
type: SIO_010056
comment: Phenotype [hp:0100252] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diaphyseal dysplasia
in dataset: phenotype

Cutaneous finger syndactyly [hp:0010554]
type: SIO_010056
comment: Phenotype [hp:0010554] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cutaneous finger syndactyly
in dataset: phenotype

Oval face [hp:0000300]
type: SIO_010056
comment: Phenotype [hp:0000300] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oval face
in dataset: phenotype

Pathologic fracture [hp:0002756]
type: SIO_010056
comment: Phenotype [hp:0002756] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pathologic fracture
in dataset: phenotype

Abnormality of the metacarpal bones [hp:0001163]
type: SIO_010056
comment: Phenotype [hp:0001163] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the metacarpal bones
in dataset: phenotype

Telangiectases in sun-exposed and nonexposed skin [hp:0007561]
type: SIO_010056
comment: Phenotype [hp:0007561] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Telangiectases in sun-exposed and nonexposed skin
in dataset: phenotype

Breech presentation [hp:0001623]
type: SIO_010056
comment: Phenotype [hp:0001623] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Breech presentation
in dataset: phenotype

Schistocytosis [hp:0001981]
type: SIO_010056
comment: Phenotype [hp:0001981] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Schistocytosis
in dataset: phenotype

Intracranial cystic lesion [hp:0010576]
type: SIO_010056
comment: Phenotype [hp:0010576] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intracranial cystic lesion
in dataset: phenotype

Wormian bones [hp:0002645]
type: SIO_010056
comment: Phenotype [hp:0002645] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Wormian bones
in dataset: phenotype

Carious teeth [hp:0000670]
type: SIO_010056
comment: Phenotype [hp:0000670] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Carious teeth
in dataset: phenotype

Broad ribs [hp:0000885]
type: SIO_010056
comment: Phenotype [hp:0000885] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad ribs
in dataset: phenotype

Wide anterior fontanel [hp:0000260]
type: SIO_010056
comment: Phenotype [hp:0000260] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Wide anterior fontanel
in dataset: phenotype

Rudimentary fibula [hp:0006381]
type: SIO_010056
comment: Phenotype [hp:0006381] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rudimentary fibula
in dataset: phenotype

Abnormality of the dorsal column of the spinal cord [hp:0011397]
type: SIO_010056
comment: Phenotype [hp:0011397] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the dorsal column of the spinal cord
in dataset: phenotype

Calcaneal epiphyseal stippling [hp:0004695]
type: SIO_010056
comment: Phenotype [hp:0004695] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcaneal epiphyseal stippling
in dataset: phenotype

Myoclonic spasms [hp:0003739]
type: SIO_010056
comment: Phenotype [hp:0003739] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myoclonic spasms
in dataset: phenotype

Absent pulmonary artery [hp:0004960]
type: SIO_010056
comment: Phenotype [hp:0004960] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent pulmonary artery
in dataset: phenotype

Late-onset spinocerebellar degeneration [hp:0006904]
type: SIO_010056
comment: Phenotype [hp:0006904] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Late-onset spinocerebellar degeneration
in dataset: phenotype

Camptodactyly of toe [hp:0001836]
type: SIO_010056
comment: Phenotype [hp:0001836] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Camptodactyly of toe
in dataset: phenotype

Infantile axial hypotonia [hp:0009062]
type: SIO_010056
comment: Phenotype [hp:0009062] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Infantile axial hypotonia
in dataset: phenotype

Intraretinal exudate [hp:0007989]
type: SIO_010056
comment: Phenotype [hp:0007989] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intraretinal exudate
in dataset: phenotype

Nausea and vomiting [hp:0002017]
type: SIO_010056
comment: Phenotype [hp:0002017] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nausea and vomiting
in dataset: phenotype

Midline defect of the nose [hp:0004122]
type: SIO_010056
comment: Phenotype [hp:0004122] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Midline defect of the nose
in dataset: phenotype

Multiple long-bone exostoses [hp:0005039]
type: SIO_010056
comment: Phenotype [hp:0005039] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple long-bone exostoses
in dataset: phenotype

Dysmenorrhea [hp:0100607]
type: SIO_010056
comment: Phenotype [hp:0100607] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysmenorrhea
in dataset: phenotype

Postaxial hand polydactyly [hp:0001162]
type: SIO_010056
comment: Phenotype [hp:0001162] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Postaxial hand polydactyly
in dataset: phenotype

Muscle fiber cytoplasmatic inclusion bodies [hp:0100303]
type: SIO_010056
comment: Phenotype [hp:0100303] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Muscle fiber cytoplasmatic inclusion bodies
in dataset: phenotype

Recurrent fractures [hp:0002757]
type: SIO_010056
comment: Phenotype [hp:0002757] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent fractures
in dataset: phenotype

Male pseudohermaphroditism [hp:0000037]
type: SIO_010056
comment: Phenotype [hp:0000037] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Male pseudohermaphroditism
in dataset: phenotype

Megaloblastic bone marrow [hp:0001980]
type: SIO_010056
comment: Phenotype [hp:0001980] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Megaloblastic bone marrow
in dataset: phenotype

Lack of skin elasticity [hp:0100679]
type: SIO_010056
comment: Phenotype [hp:0100679] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lack of skin elasticity
in dataset: phenotype

Salt craving [hp:0030083]
type: SIO_010056
comment: Phenotype [hp:0030083] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Salt craving
in dataset: phenotype

Dysplasia of the femoral head [hp:0010575]
type: SIO_010056
comment: Phenotype [hp:0010575] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysplasia of the femoral head
in dataset: phenotype

Deformed rib cage [hp:0000886]
type: SIO_010056
comment: Phenotype [hp:0000886] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deformed rib cage
in dataset: phenotype

Limited hip movement [hp:0008800]
type: SIO_010056
comment: Phenotype [hp:0008800] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limited hip movement
in dataset: phenotype

Central hypotonia [hp:0011398]
type: SIO_010056
comment: Phenotype [hp:0011398] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Central hypotonia
in dataset: phenotype

Retinal arteriolar constriction [hp:0008043]
type: SIO_010056
comment: Phenotype [hp:0008043] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal arteriolar constriction
in dataset: phenotype

Talipes cavus equinovarus [hp:0004696]
type: SIO_010056
comment: Phenotype [hp:0004696] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Talipes cavus equinovarus
in dataset: phenotype

Progressive bowing of long bones [hp:0006383]
type: SIO_010056
comment: Phenotype [hp:0006383] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive bowing of long bones
in dataset: phenotype

Exercise-induced myalgia [hp:0003738]
type: SIO_010056
comment: Phenotype [hp:0003738] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exercise-induced myalgia
in dataset: phenotype

Hypoplasia of the pons [hp:0012110]
type: SIO_010056
comment: Phenotype [hp:0012110] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the pons
in dataset: phenotype

Decreased serum complement factor H [hp:0005369]
type: SIO_010056
comment: Phenotype [hp:0005369] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased serum complement factor H
in dataset: phenotype

Hepatomegaly [hp:0002240]
type: SIO_010056
comment: Phenotype [hp:0002240] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatomegaly
in dataset: phenotype

Nausea [hp:0002018]
type: SIO_010056
comment: Phenotype [hp:0002018] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nausea
in dataset: phenotype

Pulmonary artery sling [hp:0004961]
type: SIO_010056
comment: Phenotype [hp:0004961] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary artery sling
in dataset: phenotype

Stress/infection-induced lactic acidosis [hp:0004897]
type: SIO_010056
comment: Phenotype [hp:0004897] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stress/infection-induced lactic acidosis
in dataset: phenotype

Progressive distal muscle weakness [hp:0009063]
type: SIO_010056
comment: Phenotype [hp:0009063] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive distal muscle weakness
in dataset: phenotype

Progressive psychomotor deterioration [hp:0007272]
type: SIO_010056
comment: Phenotype [hp:0007272] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive psychomotor deterioration
in dataset: phenotype

Bone-marrow foam cells [hp:0004333]
type: SIO_010056
comment: Phenotype [hp:0004333] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bone-marrow foam cells
in dataset: phenotype

Prolonged miniature endplate currents [hp:0003436]
type: SIO_010056
comment: Phenotype [hp:0003436] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolonged miniature endplate currents
in dataset: phenotype

Scapular muscle atrophy [hp:0009060]
type: SIO_010056
comment: Phenotype [hp:0009060] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Scapular muscle atrophy
in dataset: phenotype

Thoracic hypoplasia [hp:0005257]
type: SIO_010056
comment: Phenotype [hp:0005257] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thoracic hypoplasia
in dataset: phenotype

Episodic ketoacidosis [hp:0005974]
type: SIO_010056
comment: Phenotype [hp:0005974] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Episodic ketoacidosis
in dataset: phenotype

Slow-growing nails [hp:0008383]
type: SIO_010056
comment: Phenotype [hp:0008383] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slow-growing nails
in dataset: phenotype

Hypoalphalipoproteinemia [hp:0003233]
type: SIO_010056
comment: Phenotype [hp:0003233] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoalphalipoproteinemia
in dataset: phenotype

Extraadrenal pheochromocytoma [hp:0006737]
type: SIO_010056
comment: Phenotype [hp:0006737] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Extraadrenal pheochromocytoma
in dataset: phenotype

Rough bone trabeculation [hp:0100670]
type: SIO_010056
comment: Phenotype [hp:0100670] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rough bone trabeculation
in dataset: phenotype

Aplasia/Hypoplasia of the tongue [hp:0010295]
type: SIO_010056
comment: Phenotype [hp:0010295] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the tongue
in dataset: phenotype

Hepatic fibrosis [hp:0001395]
type: SIO_010056
comment: Phenotype [hp:0001395] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatic fibrosis
in dataset: phenotype

Clinodactyly [hp:0030084]
type: SIO_010056
comment: Phenotype [hp:0030084] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Clinodactyly
in dataset: phenotype

Cavernous hemangioma [hp:0001048]
type: SIO_010056
comment: Phenotype [hp:0001048] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cavernous hemangioma
in dataset: phenotype

Motor delay [hp:0001270]
type: SIO_010056
comment: Phenotype [hp:0001270] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Motor delay
in dataset: phenotype

Broad nasal tip [hp:0000455]
type: SIO_010056
comment: Phenotype [hp:0000455] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad nasal tip
in dataset: phenotype

Amelia [hp:0009827]
type: SIO_010056
comment: Phenotype [hp:0009827] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Amelia
in dataset: phenotype

Myelodysplasia [hp:0002863]
type: SIO_010056
comment: Phenotype [hp:0002863] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myelodysplasia
in dataset: phenotype

Methemoglobinemia [hp:0012119]
type: SIO_010056
comment: Phenotype [hp:0012119] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Methemoglobinemia
in dataset: phenotype

Abnormality of lymphocytes [hp:0004332]
type: SIO_010056
comment: Phenotype [hp:0004332] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of lymphocytes
in dataset: phenotype

Decreased plasma carnitine [hp:0003234]
type: SIO_010056
comment: Phenotype [hp:0003234] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased plasma carnitine
in dataset: phenotype

Cold-induced hand cramps [hp:0003435]
type: SIO_010056
comment: Phenotype [hp:0003435] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cold-induced hand cramps
in dataset: phenotype

Left bundle branch block [hp:0011713]
type: SIO_010056
comment: Phenotype [hp:0011713] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Left bundle branch block
in dataset: phenotype

Thickened Achilles tendon [hp:0004690]
type: SIO_010056
comment: Phenotype [hp:0004690] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thickened Achilles tendon
in dataset: phenotype

Increased IgE level [hp:0003212]
type: SIO_010056
comment: Phenotype [hp:0003212] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased IgE level
in dataset: phenotype

Pectoral muscle hypoplasia/aplasia [hp:0005258]
type: SIO_010056
comment: Phenotype [hp:0005258] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pectoral muscle hypoplasia/aplasia
in dataset: phenotype

Cortical dysplasia [hp:0002539]
type: SIO_010056
comment: Phenotype [hp:0002539] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cortical dysplasia
in dataset: phenotype

Hyperechogenic pancreas [hp:0006276]
type: SIO_010056
comment: Phenotype [hp:0006276] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperechogenic pancreas
in dataset: phenotype

Knee flexion contracture [hp:0006380]
type: SIO_010056
comment: Phenotype [hp:0006380] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Knee flexion contracture
in dataset: phenotype

Distal upper limb muscle weakness [hp:0008959]
type: SIO_010056
comment: Phenotype [hp:0008959] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Distal upper limb muscle weakness
in dataset: phenotype

Atopic dermatitis [hp:0001047]
type: SIO_010056
comment: Phenotype [hp:0001047] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atopic dermatitis
in dataset: phenotype

Cirrhosis [hp:0001394]
type: SIO_010056
comment: Phenotype [hp:0001394] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cirrhosis
in dataset: phenotype

Obesity [hp:0001513]
type: SIO_010056
comment: Phenotype [hp:0001513] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Obesity
in dataset: phenotype

Long foot [hp:0001833]
type: SIO_010056
comment: Phenotype [hp:0001833] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long foot
in dataset: phenotype

Bifid nasal tip [hp:0000456]
type: SIO_010056
comment: Phenotype [hp:0000456] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid nasal tip
in dataset: phenotype

Limb duplication [hp:0100524]
type: SIO_010056
comment: Phenotype [hp:0100524] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb duplication
in dataset: phenotype

Recurrent bacterial meningitis [hp:0007274]
type: SIO_010056
comment: Phenotype [hp:0007274] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent bacterial meningitis
in dataset: phenotype

Epispadias [hp:0000039]
type: SIO_010056
comment: Phenotype [hp:0000039] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Epispadias
in dataset: phenotype

Toxemia of pregnancy [hp:0100603]
type: SIO_010056
comment: Phenotype [hp:0100603] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Toxemia of pregnancy
in dataset: phenotype

Absent Achilles reflex [hp:0003438]
type: SIO_010056
comment: Phenotype [hp:0003438] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent Achilles reflex
in dataset: phenotype

Pulmonary arterial medial hypertrophy [hp:0004964]
type: SIO_010056
comment: Phenotype [hp:0004964] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary arterial medial hypertrophy
in dataset: phenotype

Pulmonary valve defects [hp:0005148]
type: SIO_010056
comment: Phenotype [hp:0005148] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary valve defects
in dataset: phenotype

Long second metacarpal [hp:0006040]
type: SIO_010056
comment: Phenotype [hp:0006040] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Long second metacarpal
in dataset: phenotype

Decreased skull ossification [hp:0004331]
type: SIO_010056
comment: Phenotype [hp:0004331] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased skull ossification
in dataset: phenotype

Hypermethioninemia [hp:0003235]
type: SIO_010056
comment: Phenotype [hp:0003235] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypermethioninemia
in dataset: phenotype

Decreased resting energy expenditure [hp:0012340]
type: SIO_010056
comment: Phenotype [hp:0012340] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased resting energy expenditure
in dataset: phenotype

Abnormality of femoral epiphysis [hp:0006499]
type: SIO_010056
comment: Phenotype [hp:0006499] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of femoral epiphysis
in dataset: phenotype

Renal cortical adenoma [hp:0006735]
type: SIO_010056
comment: Phenotype [hp:0006735] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal cortical adenoma
in dataset: phenotype

Abnormal facility in opposing the shoulders [hp:0005259]
type: SIO_010056
comment: Phenotype [hp:0005259] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal facility in opposing the shoulders
in dataset: phenotype

Decreased number of peripheral myelinated nerve fibers [hp:0003380]
type: SIO_010056
comment: Phenotype [hp:0003380] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased number of peripheral myelinated nerve fibers
in dataset: phenotype

2-3 toe syndactyly [hp:0004691]
type: SIO_010056
comment: Phenotype [hp:0004691] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 2-3 toe syndactyly
in dataset: phenotype

EEG with spike-wave complexes (>3.5 Hz) [hp:0010849]
type: SIO_010056
comment: Phenotype [hp:0010849] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EEG with spike-wave complexes (>3.5 Hz)
in dataset: phenotype

Androgen insufficiency [hp:0008226]
type: SIO_010056
comment: Phenotype [hp:0008226] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Androgen insufficiency
in dataset: phenotype

Abnormal cortical gyration [hp:0002536]
type: SIO_010056
comment: Phenotype [hp:0002536] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal cortical gyration
in dataset: phenotype

Proximal lower limb amyotrophy [hp:0008956]
type: SIO_010056
comment: Phenotype [hp:0008956] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal lower limb amyotrophy
in dataset: phenotype

Aplasia/Hypoplasia of the uvula [hp:0010293]
type: SIO_010056
comment: Phenotype [hp:0010293] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the uvula
in dataset: phenotype

Aplasia of the uterus [hp:0000151]
type: SIO_010056
comment: Phenotype [hp:0000151] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the uterus
in dataset: phenotype

Medullary thyroid carcinoma [hp:0002865]
type: SIO_010056
comment: Phenotype [hp:0002865] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Medullary thyroid carcinoma
in dataset: phenotype

Cerebellar atrophy [hp:0001272]
type: SIO_010056
comment: Phenotype [hp:0001272] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebellar atrophy
in dataset: phenotype

Abnormality of the foot [hp:0001760]
type: SIO_010056
comment: Phenotype [hp:0001760] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the foot
in dataset: phenotype

Phocomelia [hp:0009829]
type: SIO_010056
comment: Phenotype [hp:0009829] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Phocomelia
in dataset: phenotype

Liver abscess [hp:0100523]
type: SIO_010056
comment: Phenotype [hp:0100523] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Liver abscess
in dataset: phenotype

Abnormality of the metatarsal bones [hp:0001832]
type: SIO_010056
comment: Phenotype [hp:0001832] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the metatarsal bones
in dataset: phenotype

Hepatic steatosis [hp:0001397]
type: SIO_010056
comment: Phenotype [hp:0001397] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatic steatosis
in dataset: phenotype

Depressed nasal ridge [hp:0000457]
type: SIO_010056
comment: Phenotype [hp:0000457] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Depressed nasal ridge
in dataset: phenotype

Decreased methylmalonyl-CoA mutase activity [hp:0003210]
type: SIO_010056
comment: Phenotype [hp:0003210] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased methylmalonyl-CoA mutase activity
in dataset: phenotype

Elevated serum creatine phosphokinase [hp:0003236]
type: SIO_010056
comment: Phenotype [hp:0003236] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated serum creatine phosphokinase
in dataset: phenotype

Reduced pancreatic beta cells [hp:0006274]
type: SIO_010056
comment: Phenotype [hp:0006274] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced pancreatic beta cells
in dataset: phenotype

Fructose intolerance [hp:0005973]
type: SIO_010056
comment: Phenotype [hp:0005973] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fructose intolerance
in dataset: phenotype

4-5 toe syndactyly [hp:0004692]
type: SIO_010056
comment: Phenotype [hp:0004692] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 4-5 toe syndactyly
in dataset: phenotype

Thyroid follicular hyperplasia [hp:0008225]
type: SIO_010056
comment: Phenotype [hp:0008225] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thyroid follicular hyperplasia
in dataset: phenotype

Cholestasis [hp:0001396]
type: SIO_010056
comment: Phenotype [hp:0001396] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cholestasis
in dataset: phenotype

Gonadoblastoma [hp:0000150]
type: SIO_010056
comment: Phenotype [hp:0000150] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gonadoblastoma
in dataset: phenotype

Absent uvula [hp:0010292]
type: SIO_010056
comment: Phenotype [hp:0010292] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent uvula
in dataset: phenotype

Hypoplastic iliac wing [hp:0002866]
type: SIO_010056
comment: Phenotype [hp:0002866] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic iliac wing
in dataset: phenotype

Pes cavus [hp:0001761]
type: SIO_010056
comment: Phenotype [hp:0001761] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pes cavus
in dataset: phenotype

Y-shaped metacarpals [hp:0006042]
type: SIO_010056
comment: Phenotype [hp:0006042] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Y-shaped metacarpals
in dataset: phenotype

Anosmia [hp:0000458]
type: SIO_010056
comment: Phenotype [hp:0000458] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anosmia
in dataset: phenotype

Thymoma [hp:0100522]
type: SIO_010056
comment: Phenotype [hp:0100522] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thymoma
in dataset: phenotype

Polyneuropathy [hp:0001271]
type: SIO_010056
comment: Phenotype [hp:0001271] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polyneuropathy
in dataset: phenotype

Short toe [hp:0001831]
type: SIO_010056
comment: Phenotype [hp:0001831] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short toe
in dataset: phenotype

Hyperchloremia [hp:0011423]
type: SIO_010056
comment: Phenotype [hp:0011423] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperchloremia
in dataset: phenotype

Non-caseating epithelioid cell granulomatosis [hp:0012220]
type: SIO_010056
comment: Phenotype [hp:0012220] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Non-caseating epithelioid cell granulomatosis
in dataset: phenotype

Hypertrophic nerve changes [hp:0003382]
type: SIO_010056
comment: Phenotype [hp:0003382] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertrophic nerve changes
in dataset: phenotype

Beta-cell dysfunction [hp:0006279]
type: SIO_010056
comment: Phenotype [hp:0006279] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Beta-cell dysfunction
in dataset: phenotype

Type II diabetes mellitus [hp:0005978]
type: SIO_010056
comment: Phenotype [hp:0005978] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type II diabetes mellitus
in dataset: phenotype

Metaphyseal cupping of proximal phalanges [hp:0006208]
type: SIO_010056
comment: Phenotype [hp:0006208] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metaphyseal cupping of proximal phalanges
in dataset: phenotype

Hepatitis [hp:0012115]
type: SIO_010056
comment: Phenotype [hp:0012115] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatitis
in dataset: phenotype

Chronic tubulointerstitial nephritis [hp:0004743]
type: SIO_010056
comment: Phenotype [hp:0004743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic tubulointerstitial nephritis
in dataset: phenotype

Increased anterioposterior diameter of thorax [hp:0005253]
type: SIO_010056
comment: Phenotype [hp:0005253] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased anterioposterior diameter of thorax
in dataset: phenotype

Ventricular septal defect [hp:0001629]
type: SIO_010056
comment: Phenotype [hp:0001629] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ventricular septal defect
in dataset: phenotype

Increased testosterone [hp:0030088]
type: SIO_010056
comment: Phenotype [hp:0030088] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased testosterone
in dataset: phenotype

Postaxial foot polydactyly [hp:0001830]
type: SIO_010056
comment: Phenotype [hp:0001830] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Postaxial foot polydactyly
in dataset: phenotype

Bundle branch block [hp:0011710]
type: SIO_010056
comment: Phenotype [hp:0011710] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bundle branch block
in dataset: phenotype

Eclampsia [hp:0100601]
type: SIO_010056
comment: Phenotype [hp:0100601] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Eclampsia
in dataset: phenotype

Abnormality of the acetabulum [hp:0003170]
type: SIO_010056
comment: Phenotype [hp:0003170] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the acetabulum
in dataset: phenotype

Triangular nasal tip [hp:0000451]
type: SIO_010056
comment: Phenotype [hp:0000451] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular nasal tip
in dataset: phenotype

Talipes equinovarus [hp:0001762]
type: SIO_010056
comment: Phenotype [hp:0001762] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Talipes equinovarus
in dataset: phenotype

Agenesis of corpus callosum [hp:0001274]
type: SIO_010056
comment: Phenotype [hp:0001274] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Agenesis of corpus callosum
in dataset: phenotype

Neoplasm of the thymus [hp:0100521]
type: SIO_010056
comment: Phenotype [hp:0100521] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neoplasm of the thymus
in dataset: phenotype

Abnormality of dentin [hp:0010299]
type: SIO_010056
comment: Phenotype [hp:0010299] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of dentin
in dataset: phenotype

Cardiac myxoma [hp:0011672]
type: SIO_010056
comment: Phenotype [hp:0011672] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cardiac myxoma
in dataset: phenotype

Abnormality of the toenails [hp:0008388]
type: SIO_010056
comment: Phenotype [hp:0008388] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the toenails
in dataset: phenotype

Onion bulb formation [hp:0003383]
type: SIO_010056
comment: Phenotype [hp:0003383] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Onion bulb formation
in dataset: phenotype

Bidirectional ventricular ectopy [hp:0005147]
type: SIO_010056
comment: Phenotype [hp:0005147] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bidirectional ventricular ectopy
in dataset: phenotype

Decreased motor nerve conduction velocity [hp:0003431]
type: SIO_010056
comment: Phenotype [hp:0003431] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased motor nerve conduction velocity
in dataset: phenotype

Myelin outfoldings [hp:0004336]
type: SIO_010056
comment: Phenotype [hp:0004336] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Myelin outfoldings
in dataset: phenotype

Metabolic ketoacidosis [hp:0005979]
type: SIO_010056
comment: Phenotype [hp:0005979] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metabolic ketoacidosis
in dataset: phenotype

Gait instability, worse in the dark [hp:0006962]
type: SIO_010056
comment: Phenotype [hp:0006962] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gait instability, worse in the dark
in dataset: phenotype

Abnormality of the renal collecting system [hp:0004742]
type: SIO_010056
comment: Phenotype [hp:0004742] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the renal collecting system
in dataset: phenotype

Vertical clivus [hp:0010559]
type: SIO_010056
comment: Phenotype [hp:0010559] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vertical clivus
in dataset: phenotype

Pretibial blistering [hp:0012221]
type: SIO_010056
comment: Phenotype [hp:0012221] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pretibial blistering
in dataset: phenotype

Partial fusion of carpals [hp:0006207]
type: SIO_010056
comment: Phenotype [hp:0006207] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Partial fusion of carpals
in dataset: phenotype

Unilateral chest hypoplasia [hp:0005254]
type: SIO_010056
comment: Phenotype [hp:0005254] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral chest hypoplasia
in dataset: phenotype

Preeclampsia [hp:0100602]
type: SIO_010056
comment: Phenotype [hp:0100602] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Preeclampsia
in dataset: phenotype

Squamous cell carcinoma [hp:0002860]
type: SIO_010056
comment: Phenotype [hp:0002860] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Squamous cell carcinoma
in dataset: phenotype

Abnormality of the corpus callosum [hp:0001273]
type: SIO_010056
comment: Phenotype [hp:0001273] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the corpus callosum
in dataset: phenotype

Upper limb undergrowth [hp:0009824]
type: SIO_010056
comment: Phenotype [hp:0009824] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Upper limb undergrowth
in dataset: phenotype

Smooth tongue [hp:0010298]
type: SIO_010056
comment: Phenotype [hp:0010298] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Smooth tongue
in dataset: phenotype

Progressive cervical vertebral spine fusion [hp:0008449]
type: SIO_010056
comment: Phenotype [hp:0008449] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive cervical vertebral spine fusion
in dataset: phenotype

Pes planus [hp:0001763]
type: SIO_010056
comment: Phenotype [hp:0001763] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pes planus
in dataset: phenotype

Choanal stenosis [hp:0000452]
type: SIO_010056
comment: Phenotype [hp:0000452] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Choanal stenosis
in dataset: phenotype

Hypertension associated with pheochromocytoma [hp:0002640]
type: SIO_010056
comment: Phenotype [hp:0002640] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertension associated with pheochromocytoma
in dataset: phenotype

Nasal, dysarthic speech [hp:0008376]
type: SIO_010056
comment: Phenotype [hp:0008376] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nasal, dysarthic speech
in dataset: phenotype

Progressive distal muscular atrophy [hp:0008955]
type: SIO_010056
comment: Phenotype [hp:0008955] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive distal muscular atrophy
in dataset: phenotype

Aplasia of the pectoralis major muscle [hp:0009751]
type: SIO_010056
comment: Phenotype [hp:0009751] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia of the pectoralis major muscle
in dataset: phenotype

Compensated hypothyroidism [hp:0008223]
type: SIO_010056
comment: Phenotype [hp:0008223] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Compensated hypothyroidism
in dataset: phenotype

Decreased amplitude of sensory action potentials [hp:0007078]
type: SIO_010056
comment: Phenotype [hp:0007078] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased amplitude of sensory action potentials
in dataset: phenotype

Peripheral axonal atrophy [hp:0003384]
type: SIO_010056
comment: Phenotype [hp:0003384] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral axonal atrophy
in dataset: phenotype

Squamous cell carcinoma of the skin [hp:0006739]
type: SIO_010056
comment: Phenotype [hp:0006739] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Squamous cell carcinoma of the skin
in dataset: phenotype

Concentric narrowing of visual fields [hp:0007981]
type: SIO_010056
comment: Phenotype [hp:0007981] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Concentric narrowing of visual fields
in dataset: phenotype

Left ventricular septal hypertrophy [hp:0005144]
type: SIO_010056
comment: Phenotype [hp:0005144] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Left ventricular septal hypertrophy
in dataset: phenotype

Hypertyrosinemia [hp:0003231]
type: SIO_010056
comment: Phenotype [hp:0003231] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertyrosinemia
in dataset: phenotype

Thick corpus callosum [hp:0007074]
type: SIO_010056
comment: Phenotype [hp:0007074] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thick corpus callosum
in dataset: phenotype

Hyperkalemic metabolic acidosis [hp:0005976]
type: SIO_010056
comment: Phenotype [hp:0005976] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperkalemic metabolic acidosis
in dataset: phenotype

Pancreatic hyperplasia [hp:0006277]
type: SIO_010056
comment: Phenotype [hp:0006277] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pancreatic hyperplasia
in dataset: phenotype

Generalized microdontia [hp:0006311]
type: SIO_010056
comment: Phenotype [hp:0006311] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized microdontia
in dataset: phenotype

Absence of pectoralis minor muscle [hp:0005255]
type: SIO_010056
comment: Phenotype [hp:0005255] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of pectoralis minor muscle
in dataset: phenotype

Juvenile cortical cataract [hp:0007876]
type: SIO_010056
comment: Phenotype [hp:0007876] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Juvenile cortical cataract
in dataset: phenotype

Hypersegmentation of proximal phalanx of second finger [hp:0006206]
type: SIO_010056
comment: Phenotype [hp:0006206] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypersegmentation of proximal phalanx of second finger
in dataset: phenotype

Right bundle branch block [hp:0011712]
type: SIO_010056
comment: Phenotype [hp:0011712] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Right bundle branch block
in dataset: phenotype

Arachnoid hemangiomatosis [hp:0012222]
type: SIO_010056
comment: Phenotype [hp:0012222] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arachnoid hemangiomatosis
in dataset: phenotype

Small for gestational age [hp:0001518]
type: SIO_010056
comment: Phenotype [hp:0001518] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Small for gestational age
in dataset: phenotype

Recurrent cerebral hemorrhage [hp:0004968]
type: SIO_010056
comment: Phenotype [hp:0004968] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent cerebral hemorrhage
in dataset: phenotype

Atypical absence seizures [hp:0007270]
type: SIO_010056
comment: Phenotype [hp:0007270] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Atypical absence seizures
in dataset: phenotype

Granular osmiophilic deposits (GROD) in cells [hp:0003657]
type: SIO_010056
comment: Phenotype [hp:0003657] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Granular osmiophilic deposits (GROD) in cells
in dataset: phenotype

Sensory ataxic neuropathy [hp:0003434]
type: SIO_010056
comment: Phenotype [hp:0003434] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sensory ataxic neuropathy
in dataset: phenotype

Jerky head movements [hp:0006961]
type: SIO_010056
comment: Phenotype [hp:0006961] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Jerky head movements
in dataset: phenotype

Bifid tongue [hp:0010297]
type: SIO_010056
comment: Phenotype [hp:0010297] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid tongue
in dataset: phenotype

Shoulder muscle hypoplasia [hp:0008952]
type: SIO_010056
comment: Phenotype [hp:0008952] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shoulder muscle hypoplasia
in dataset: phenotype

Vaginal hernia [hp:0100672]
type: SIO_010056
comment: Phenotype [hp:0100672] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vaginal hernia
in dataset: phenotype

Choanal atresia [hp:0000453]
type: SIO_010056
comment: Phenotype [hp:0000453] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Choanal atresia
in dataset: phenotype

Melanoma [hp:0002861]
type: SIO_010056
comment: Phenotype [hp:0002861] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Melanoma
in dataset: phenotype

Aplasia/Hypoplasia of the nails [hp:0008386]
type: SIO_010056
comment: Phenotype [hp:0008386] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the nails
in dataset: phenotype

Inflexible adherence to routines or rituals [hp:0000732]
type: SIO_010056
comment: Phenotype [hp:0000732] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Inflexible adherence to routines or rituals
in dataset: phenotype

Female infertility [hp:0008222]
type: SIO_010056
comment: Phenotype [hp:0008222] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Female infertility
in dataset: phenotype

Cleft in skull base [hp:0009752]
type: SIO_010056
comment: Phenotype [hp:0009752] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cleft in skull base
in dataset: phenotype

Hypertonia [hp:0001276]
type: SIO_010056
comment: Phenotype [hp:0001276] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertonia
in dataset: phenotype

Hypochloremic metabolic alkalosis [hp:0005977]
type: SIO_010056
comment: Phenotype [hp:0005977] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypochloremic metabolic alkalosis
in dataset: phenotype

Absent retinal pigment epithelium [hp:0007980]
type: SIO_010056
comment: Phenotype [hp:0007980] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent retinal pigment epithelium
in dataset: phenotype

Abnormality of the wrist [hp:0003019]
type: SIO_010056
comment: Phenotype [hp:0003019] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the wrist
in dataset: phenotype

Coronary artery stenosis [hp:0005145]
type: SIO_010056
comment: Phenotype [hp:0005145] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coronary artery stenosis
in dataset: phenotype

Mitochondrial malic enzyme reduced [hp:0003232]
type: SIO_010056
comment: Phenotype [hp:0003232] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mitochondrial malic enzyme reduced
in dataset: phenotype

Dermal atrophy [hp:0004334]
type: SIO_010056
comment: Phenotype [hp:0004334] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dermal atrophy
in dataset: phenotype

Congenital blindness [hp:0007875]
type: SIO_010056
comment: Phenotype [hp:0007875] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital blindness
in dataset: phenotype

Ectopic pancreatic tissue [hp:0006278]
type: SIO_010056
comment: Phenotype [hp:0006278] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopic pancreatic tissue
in dataset: phenotype

Unilateral absence of pectoralis major muscle [hp:0005256]
type: SIO_010056
comment: Phenotype [hp:0005256] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral absence of pectoralis major muscle
in dataset: phenotype

Splenic rupture [hp:0012223]
type: SIO_010056
comment: Phenotype [hp:0012223] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Splenic rupture
in dataset: phenotype

Decreased serum ferritin [hp:0012343]
type: SIO_010056
comment: Phenotype [hp:0012343] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased serum ferritin
in dataset: phenotype

Laryngeal carcinoma [hp:0012118]
type: SIO_010056
comment: Phenotype [hp:0012118] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Laryngeal carcinoma
in dataset: phenotype

Occipital myelomeningocele [hp:0007271]
type: SIO_010056
comment: Phenotype [hp:0007271] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Occipital myelomeningocele
in dataset: phenotype

Elevated serum long-chain fatty acids [hp:0045016]
type: SIO_010056
comment: Phenotype [hp:0045016] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated serum long-chain fatty acids
in dataset: phenotype

Disproportionate tall stature [hp:0001519]
type: SIO_010056
comment: Phenotype [hp:0001519] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Disproportionate tall stature
in dataset: phenotype

Choroid plexus calcification [hp:0006960]
type: SIO_010056
comment: Phenotype [hp:0006960] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Choroid plexus calcification
in dataset: phenotype

Hypomethioninemia [hp:0003658]
type: SIO_010056
comment: Phenotype [hp:0003658] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypomethioninemia
in dataset: phenotype

Flared nostrils [hp:0000454]
type: SIO_010056
comment: Phenotype [hp:0000454] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flared nostrils
in dataset: phenotype

Limb undergrowth [hp:0009826]
type: SIO_010056
comment: Phenotype [hp:0009826] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb undergrowth
in dataset: phenotype

Peripheral pulmonary artery stenosis [hp:0004969]
type: SIO_010056
comment: Phenotype [hp:0004969] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral pulmonary artery stenosis
in dataset: phenotype

Pectoralis major hypoplasia [hp:0008953]
type: SIO_010056
comment: Phenotype [hp:0008953] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pectoralis major hypoplasia
in dataset: phenotype

Ankyloglossia [hp:0010296]
type: SIO_010056
comment: Phenotype [hp:0010296] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ankyloglossia
in dataset: phenotype

Arrhythmia [hp:0011675]
type: SIO_010056
comment: Phenotype [hp:0011675] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arrhythmia
in dataset: phenotype

Bladder carcinoma [hp:0002862]
type: SIO_010056
comment: Phenotype [hp:0002862] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bladder carcinoma
in dataset: phenotype

Hammertoe [hp:0001765]
type: SIO_010056
comment: Phenotype [hp:0001765] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hammertoe
in dataset: phenotype

Left anterior fascicular block [hp:0011711]
type: SIO_010056
comment: Phenotype [hp:0011711] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Left anterior fascicular block
in dataset: phenotype

Extrapyramidal muscular rigidity [hp:0007076]
type: SIO_010056
comment: Phenotype [hp:0007076] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Extrapyramidal muscular rigidity
in dataset: phenotype

Stereotypic behavior [hp:0000733]
type: SIO_010056
comment: Phenotype [hp:0000733] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Stereotypic behavior
in dataset: phenotype

Abnormal trabecular bone morphology [hp:0100671]
type: SIO_010056
comment: Phenotype [hp:0100671] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal trabecular bone morphology
in dataset: phenotype

Abnormal posturing [hp:0002533]
type: SIO_010056
comment: Phenotype [hp:0002533] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal posturing
in dataset: phenotype

Hypoplastic coccygeal vertebrae [hp:0008447]
type: SIO_010056
comment: Phenotype [hp:0008447] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic coccygeal vertebrae
in dataset: phenotype

Adrenal hyperplasia [hp:0008221]
type: SIO_010056
comment: Phenotype [hp:0008221] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adrenal hyperplasia
in dataset: phenotype

Abnormality of the liver [hp:0001392]
type: SIO_010056
comment: Phenotype [hp:0001392] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the liver
in dataset: phenotype

T-wave inversion in the right precordial leads [hp:0003140]
type: SIO_010056
comment: Phenotype [hp:0003140] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: T-wave inversion in the right precordial leads
in dataset: phenotype

Abnormality of vision evoked potentials [hp:0000649]
type: SIO_010056
comment: Phenotype [hp:0000649] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of vision evoked potentials
in dataset: phenotype

Large posterior fontanelle [hp:0004491]
type: SIO_010056
comment: Phenotype [hp:0004491] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large posterior fontanelle
in dataset: phenotype

Type 1 muscle fiber atrophy [hp:0011807]
type: SIO_010056
comment: Phenotype [hp:0011807] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type 1 muscle fiber atrophy
in dataset: phenotype

Calcification of falx cerebri [hp:0005462]
type: SIO_010056
comment: Phenotype [hp:0005462] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcification of falx cerebri
in dataset: phenotype

Prominent nasal bridge [hp:0000426]
type: SIO_010056
comment: Phenotype [hp:0000426] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent nasal bridge
in dataset: phenotype

Calcific aortic valve stenosis [hp:0005173]
type: SIO_010056
comment: Phenotype [hp:0005173] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calcific aortic valve stenosis
in dataset: phenotype

Benign genitourinary tract neoplasm [hp:0006778]
type: SIO_010056
comment: Phenotype [hp:0006778] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Benign genitourinary tract neoplasm
in dataset: phenotype

Immotile cilia [hp:0012263]
type: SIO_010056
comment: Phenotype [hp:0012263] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Immotile cilia
in dataset: phenotype

Neuronal loss in central nervous system [hp:0002529]
type: SIO_010056
comment: Phenotype [hp:0002529] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neuronal loss in central nervous system
in dataset: phenotype

Narrow vertebral interpedicular distance [hp:0008450]
type: SIO_010056
comment: Phenotype [hp:0008450] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow vertebral interpedicular distance
in dataset: phenotype

Lower limb spasticity [hp:0002061]
type: SIO_010056
comment: Phenotype [hp:0002061] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lower limb spasticity
in dataset: phenotype

Intestinal pseudo-obstruction [hp:0004389]
type: SIO_010056
comment: Phenotype [hp:0004389] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intestinal pseudo-obstruction
in dataset: phenotype

Congenital septal defect [hp:0004760]
type: SIO_010056
comment: Phenotype [hp:0004760] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital septal defect
in dataset: phenotype

Foveal dystrophy [hp:0007798]
type: SIO_010056
comment: Phenotype [hp:0007798] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Foveal dystrophy
in dataset: phenotype

Posterior vertebral hypoplasia [hp:0008451]
type: SIO_010056
comment: Phenotype [hp:0008451] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior vertebral hypoplasia
in dataset: phenotype

Left postterior fascicular block [hp:0005172]
type: SIO_010056
comment: Phenotype [hp:0005172] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Left postterior fascicular block
in dataset: phenotype

Cogwheel rigidity [hp:0002396]
type: SIO_010056
comment: Phenotype [hp:0002396] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cogwheel rigidity
in dataset: phenotype

Partial albinism [hp:0007443]
type: SIO_010056
comment: Phenotype [hp:0007443] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Partial albinism
in dataset: phenotype

Calvarial hyperostosis [hp:0004490]
type: SIO_010056
comment: Phenotype [hp:0004490] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Calvarial hyperostosis
in dataset: phenotype

Coarse hair [hp:0002208]
type: SIO_010056
comment: Phenotype [hp:0002208] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Coarse hair
in dataset: phenotype

Dysplastic iliac wings [hp:0008794]
type: SIO_010056
comment: Phenotype [hp:0008794] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysplastic iliac wings
in dataset: phenotype

Microcolon [hp:0004388]
type: SIO_010056
comment: Phenotype [hp:0004388] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Microcolon
in dataset: phenotype

Conjunctival whitish salt-like deposits [hp:0007799]
type: SIO_010056
comment: Phenotype [hp:0007799] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Conjunctival whitish salt-like deposits
in dataset: phenotype

Diffuse reticular or finely nodular infiltrations [hp:0002207]
type: SIO_010056
comment: Phenotype [hp:0002207] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse reticular or finely nodular infiltrations
in dataset: phenotype

Hyperbetalipoproteinemia [hp:0003141]
type: SIO_010056
comment: Phenotype [hp:0003141] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperbetalipoproteinemia
in dataset: phenotype

Widely patent fontanelles and sutures [hp:0004492]
type: SIO_010056
comment: Phenotype [hp:0004492] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Widely patent fontanelles and sutures
in dataset: phenotype

Epicanthus inversus [hp:0000537]
type: SIO_010056
comment: Phenotype [hp:0000537] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Epicanthus inversus
in dataset: phenotype

Craniofacial disproportion [hp:0005461]
type: SIO_010056
comment: Phenotype [hp:0005461] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Craniofacial disproportion
in dataset: phenotype

Abnormal ciliary motility [hp:0012262]
type: SIO_010056
comment: Phenotype [hp:0012262] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal ciliary motility
in dataset: phenotype

Abnormal number of teeth [hp:0006483]
type: SIO_010056
comment: Phenotype [hp:0006483] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal number of teeth
in dataset: phenotype

Alveolar rhabdomyosarcoma [hp:0006779]
type: SIO_010056
comment: Phenotype [hp:0006779] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Alveolar rhabdomyosarcoma
in dataset: phenotype

Prominent epicanthal folds [hp:0007930]
type: SIO_010056
comment: Phenotype [hp:0007930] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent epicanthal folds
in dataset: phenotype

Granulovacuolar degeneration [hp:0002528]
type: SIO_010056
comment: Phenotype [hp:0002528] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Granulovacuolar degeneration
in dataset: phenotype

Morphological abnormality of the pyramidal tract [hp:0002062]
type: SIO_010056
comment: Phenotype [hp:0002062] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Morphological abnormality of the pyramidal tract
in dataset: phenotype

Vivid hallucinations [hp:0006803]
type: SIO_010056
comment: Phenotype [hp:0006803] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Vivid hallucinations
in dataset: phenotype

Post-angioplasty coronary artery restenosis [hp:0004761]
type: SIO_010056
comment: Phenotype [hp:0004761] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Post-angioplasty coronary artery restenosis
in dataset: phenotype

Subungual fibromas [hp:0009724]
type: SIO_010056
comment: Phenotype [hp:0009724] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subungual fibromas
in dataset: phenotype

Congenital primary aphakia [hp:0007707]
type: SIO_010056
comment: Phenotype [hp:0007707] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital primary aphakia
in dataset: phenotype

Pulmonary fibrosis [hp:0002206]
type: SIO_010056
comment: Phenotype [hp:0002206] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary fibrosis
in dataset: phenotype

Pseudopapilledema [hp:0000538]
type: SIO_010056
comment: Phenotype [hp:0000538] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pseudopapilledema
in dataset: phenotype

Craniofacial hyperostosis [hp:0004493]
type: SIO_010056
comment: Phenotype [hp:0004493] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Craniofacial hyperostosis
in dataset: phenotype

Enterocolitis [hp:0004387]
type: SIO_010056
comment: Phenotype [hp:0004387] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enterocolitis
in dataset: phenotype

Polyarticular arthritis [hp:0005764]
type: SIO_010056
comment: Phenotype [hp:0005764] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polyarticular arthritis
in dataset: phenotype

Multiple enchondromatosis [hp:0005701]
type: SIO_010056
comment: Phenotype [hp:0005701] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple enchondromatosis
in dataset: phenotype

Broad distal phalanx of the hallux [hp:0010077]
type: SIO_010056
comment: Phenotype [hp:0010077] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad distal phalanx of the hallux
in dataset: phenotype

Enlarged joints [hp:0003037]
type: SIO_010056
comment: Phenotype [hp:0003037] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged joints
in dataset: phenotype

Paradoxical myotonia [hp:0011809]
type: SIO_010056
comment: Phenotype [hp:0011809] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paradoxical myotonia
in dataset: phenotype

Congenital kyphoscoliosis [hp:0008453]
type: SIO_010056
comment: Phenotype [hp:0008453] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital kyphoscoliosis
in dataset: phenotype

Childhood-onset truncal obesity [hp:0008915]
type: SIO_010056
comment: Phenotype [hp:0008915] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Childhood-onset truncal obesity
in dataset: phenotype

Slurred speech [hp:0001350]
type: SIO_010056
comment: Phenotype [hp:0001350] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slurred speech
in dataset: phenotype

Athetosis [hp:0002305]
type: SIO_010056
comment: Phenotype [hp:0002305] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Athetosis
in dataset: phenotype

J-shaped sella turcica [hp:0002680]
type: SIO_010056
comment: Phenotype [hp:0002680] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: J-shaped sella turcica
in dataset: phenotype

Externally rotated hips [hp:0008796]
type: SIO_010056
comment: Phenotype [hp:0008796] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Externally rotated hips
in dataset: phenotype

Recurrent respiratory infections [hp:0002205]
type: SIO_010056
comment: Phenotype [hp:0002205] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent respiratory infections
in dataset: phenotype

Abnormality of refraction [hp:0000539]
type: SIO_010056
comment: Phenotype [hp:0000539] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of refraction
in dataset: phenotype

Punctate cataract [hp:0007648]
type: SIO_010056
comment: Phenotype [hp:0007648] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Punctate cataract
in dataset: phenotype

Cardiorespiratory arrest [hp:0006543]
type: SIO_010056
comment: Phenotype [hp:0006543] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cardiorespiratory arrest
in dataset: phenotype

Abnormal central microtubular pair morphology of respiratory motile cilia [hp:0012260]
type: SIO_010056
comment: Phenotype [hp:0012260] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal central microtubular pair morphology of respiratory motile cilia
in dataset: phenotype

Cerebral white matter atrophy [hp:0012762]
type: SIO_010056
comment: Phenotype [hp:0012762] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral white matter atrophy
in dataset: phenotype

Congenital microcephaly [hp:0011451]
type: SIO_010056
comment: Phenotype [hp:0011451] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital microcephaly
in dataset: phenotype

Abnormality of the cerebrum [hp:0002060]
type: SIO_010056
comment: Phenotype [hp:0002060] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the cerebrum
in dataset: phenotype

Decreased patellar reflex [hp:0011808]
type: SIO_010056
comment: Phenotype [hp:0011808] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased patellar reflex
in dataset: phenotype

Fibular hypoplasia [hp:0003038]
type: SIO_010056
comment: Phenotype [hp:0003038] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fibular hypoplasia
in dataset: phenotype

Agenesis of incisor [hp:0006485]
type: SIO_010056
comment: Phenotype [hp:0006485] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Agenesis of incisor
in dataset: phenotype

Lumbar kyphosis [hp:0008454]
type: SIO_010056
comment: Phenotype [hp:0008454] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lumbar kyphosis
in dataset: phenotype

Jerk-locked premyoclonus spikes [hp:0001351]
type: SIO_010056
comment: Phenotype [hp:0001351] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Jerk-locked premyoclonus spikes
in dataset: phenotype

Dental enamel pits [hp:0009722]
type: SIO_010056
comment: Phenotype [hp:0009722] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dental enamel pits
in dataset: phenotype

Akinesia [hp:0002304]
type: SIO_010056
comment: Phenotype [hp:0002304] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Akinesia
in dataset: phenotype

Hypointensity of cerebral white matter on MRI [hp:0007103]
type: SIO_010056
comment: Phenotype [hp:0007103] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypointensity of cerebral white matter on MRI
in dataset: phenotype

Broad distal hallux [hp:0008111]
type: SIO_010056
comment: Phenotype [hp:0008111] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad distal hallux
in dataset: phenotype

Abnormal head movements [hp:0002457]
type: SIO_010056
comment: Phenotype [hp:0002457] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal head movements
in dataset: phenotype

Demyelinating motor neuropathy [hp:0007220]
type: SIO_010056
comment: Phenotype [hp:0007220] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Demyelinating motor neuropathy
in dataset: phenotype

Palmoplantar blistering [hp:0007446]
type: SIO_010056
comment: Phenotype [hp:0007446] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palmoplantar blistering
in dataset: phenotype

Lower limb hyperreflexia [hp:0002395]
type: SIO_010056
comment: Phenotype [hp:0002395] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lower limb hyperreflexia
in dataset: phenotype

Early ossification of capital femoral epiphyses [hp:0008797]
type: SIO_010056
comment: Phenotype [hp:0008797] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Early ossification of capital femoral epiphyses
in dataset: phenotype

Premature arteriosclerosis [hp:0005177]
type: SIO_010056
comment: Phenotype [hp:0005177] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature arteriosclerosis
in dataset: phenotype

Abnormal hand morphology [hp:0005922]
type: SIO_010056
comment: Phenotype [hp:0005922] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal hand morphology
in dataset: phenotype

Drooling [hp:0002307]
type: SIO_010056
comment: Phenotype [hp:0002307] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Drooling
in dataset: phenotype

Alobar holoprosencephaly [hp:0006988]
type: SIO_010056
comment: Phenotype [hp:0006988] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Alobar holoprosencephaly
in dataset: phenotype

Protracted diarrhea [hp:0004385]
type: SIO_010056
comment: Phenotype [hp:0004385] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Protracted diarrhea
in dataset: phenotype

Frontal bone hypoplasia [hp:0005466]
type: SIO_010056
comment: Phenotype [hp:0005466] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontal bone hypoplasia
in dataset: phenotype

Bifid nose [hp:0011803]
type: SIO_010056
comment: Phenotype [hp:0011803] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid nose
in dataset: phenotype

Corneal degeneration [hp:0007705]
type: SIO_010056
comment: Phenotype [hp:0007705] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corneal degeneration
in dataset: phenotype

Ovarian papillary adenocarcinoma [hp:0006774]
type: SIO_010056
comment: Phenotype [hp:0006774] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ovarian papillary adenocarcinoma
in dataset: phenotype

Thin anteverted nares [hp:0004495]
type: SIO_010056
comment: Phenotype [hp:0004495] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Thin anteverted nares
in dataset: phenotype

Congenital hypertrophy of retinal pigment epithelium [hp:0007649]
type: SIO_010056
comment: Phenotype [hp:0007649] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital hypertrophy of retinal pigment epithelium
in dataset: phenotype

Progressive truncal ataxia [hp:0007221]
type: SIO_010056
comment: Phenotype [hp:0007221] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive truncal ataxia
in dataset: phenotype

Chorioretinal abnormality [hp:0000532]
type: SIO_010056
comment: Phenotype [hp:0000532] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chorioretinal abnormality
in dataset: phenotype

Renal dysplasia [hp:0000110]
type: SIO_010056
comment: Phenotype [hp:0000110] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal dysplasia
in dataset: phenotype

Diffuse palmoplantar hyperkeratosis [hp:0007447]
type: SIO_010056
comment: Phenotype [hp:0007447] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse palmoplantar hyperkeratosis
in dataset: phenotype

Cerebral hypomyelination [hp:0006808]
type: SIO_010056
comment: Phenotype [hp:0006808] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cerebral hypomyelination
in dataset: phenotype

Conjunctival hamartoma [hp:0100780]
type: SIO_010056
comment: Phenotype [hp:0100780] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Conjunctival hamartoma
in dataset: phenotype

Intellectual disability, severe [hp:0010864]
type: SIO_010056
comment: Phenotype [hp:0010864] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intellectual disability, severe
in dataset: phenotype

Iris atrophy [hp:0001089]
type: SIO_010056
comment: Phenotype [hp:0001089] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Iris atrophy
in dataset: phenotype

Shagreen patch [hp:0009721]
type: SIO_010056
comment: Phenotype [hp:0009721] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shagreen patch
in dataset: phenotype

Gait ataxia [hp:0002066]
type: SIO_010056
comment: Phenotype [hp:0002066] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gait ataxia
in dataset: phenotype

Loss of eyelashes [hp:0011457]
type: SIO_010056
comment: Phenotype [hp:0011457] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Loss of eyelashes
in dataset: phenotype

Dysplastic aortic valve [hp:0005176]
type: SIO_010056
comment: Phenotype [hp:0005176] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysplastic aortic valve
in dataset: phenotype

Impotence [hp:0000802]
type: SIO_010056
comment: Phenotype [hp:0000802] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impotence
in dataset: phenotype

Dysplastic corpus callosum [hp:0006989]
type: SIO_010056
comment: Phenotype [hp:0006989] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysplastic corpus callosum
in dataset: phenotype

Supernumerary ribs [hp:0005815]
type: SIO_010056
comment: Phenotype [hp:0005815] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Supernumerary ribs
in dataset: phenotype

Oppositional defiant disorder [hp:0010865]
type: SIO_010056
comment: Phenotype [hp:0010865] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oppositional defiant disorder
in dataset: phenotype

Hamartoma of tongue [hp:0011802]
type: SIO_010056
comment: Phenotype [hp:0011802] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hamartoma of tongue
in dataset: phenotype

Facial hyperostosis [hp:0005465]
type: SIO_010056
comment: Phenotype [hp:0005465] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial hyperostosis
in dataset: phenotype

Opisthotonus [hp:0002179]
type: SIO_010056
comment: Phenotype [hp:0002179] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Opisthotonus
in dataset: phenotype

Abnormality of the nasal alae [hp:0000429]
type: SIO_010056
comment: Phenotype [hp:0000429] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the nasal alae
in dataset: phenotype

Posterior choanal atresia [hp:0004496]
type: SIO_010056
comment: Phenotype [hp:0004496] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Posterior choanal atresia
in dataset: phenotype

Paroxysmal involuntary eye movements [hp:0007704]
type: SIO_010056
comment: Phenotype [hp:0007704] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Paroxysmal involuntary eye movements
in dataset: phenotype

Multiple myeloma [hp:0006775]
type: SIO_010056
comment: Phenotype [hp:0006775] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple myeloma
in dataset: phenotype

Limb dystonia [hp:0002451]
type: SIO_010056
comment: Phenotype [hp:0002451] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Limb dystonia
in dataset: phenotype

Renal juxtaglomerular cell hypertrophy/hyperplasia [hp:0000111]
type: SIO_010056
comment: Phenotype [hp:0000111] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal juxtaglomerular cell hypertrophy/hyperplasia
in dataset: phenotype

Plagiocephaly [hp:0001357]
type: SIO_010056
comment: Phenotype [hp:0001357] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Plagiocephaly
in dataset: phenotype

Chorioretinal atrophy [hp:0000533]
type: SIO_010056
comment: Phenotype [hp:0000533] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chorioretinal atrophy
in dataset: phenotype

Abnormality of the sacroiliac joint [hp:0100781]
type: SIO_010056
comment: Phenotype [hp:0100781] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the sacroiliac joint
in dataset: phenotype

C2-C3 subluxation [hp:0008456]
type: SIO_010056
comment: Phenotype [hp:0008456] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: C2-C3 subluxation
in dataset: phenotype

Hyperkeratosis over edematous areas [hp:0007448]
type: SIO_010056
comment: Phenotype [hp:0007448] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperkeratosis over edematous areas
in dataset: phenotype

Short middle phalanx of the 2nd finger [hp:0009577]
type: SIO_010056
comment: Phenotype [hp:0009577] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short middle phalanx of the 2nd finger
in dataset: phenotype

Adenoma sebaceum [hp:0009720]
type: SIO_010056
comment: Phenotype [hp:0009720] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Adenoma sebaceum
in dataset: phenotype

Corneal ulceration [hp:0012804]
type: SIO_010056
comment: Phenotype [hp:0012804] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corneal ulceration
in dataset: phenotype

Rigidity [hp:0002063]
type: SIO_010056
comment: Phenotype [hp:0002063] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rigidity
in dataset: phenotype

Spinal cord compression [hp:0002176]
type: SIO_010056
comment: Phenotype [hp:0002176] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinal cord compression
in dataset: phenotype

Prominent eyelashes [hp:0011231]
type: SIO_010056
comment: Phenotype [hp:0011231] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent eyelashes
in dataset: phenotype

Abnormality of dental morphology [hp:0006482]
type: SIO_010056
comment: Phenotype [hp:0006482] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of dental morphology
in dataset: phenotype

Hypoplastic left heart [hp:0004383]
type: SIO_010056
comment: Phenotype [hp:0004383] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic left heart
in dataset: phenotype

Abnormal retinal pigmentation [hp:0007703]
type: SIO_010056
comment: Phenotype [hp:0007703] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal retinal pigmentation
in dataset: phenotype

Craniofacial osteosclerosis [hp:0005464]
type: SIO_010056
comment: Phenotype [hp:0005464] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Craniofacial osteosclerosis
in dataset: phenotype

Abnormality of the eyebrow [hp:0000534]
type: SIO_010056
comment: Phenotype [hp:0000534] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the eyebrow
in dataset: phenotype

Prominent occiput [hp:0000269]
type: SIO_010056
comment: Phenotype [hp:0000269] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prominent occiput
in dataset: phenotype

Congenital glaucoma [hp:0001087]
type: SIO_010056
comment: Phenotype [hp:0001087] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital glaucoma
in dataset: phenotype

Abnormality of primary teeth [hp:0006481]
type: SIO_010056
comment: Phenotype [hp:0006481] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of primary teeth
in dataset: phenotype

Eye of the tiger anomaly of globus pallidus [hp:0002454]
type: SIO_010056
comment: Phenotype [hp:0002454] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Eye of the tiger anomaly of globus pallidus
in dataset: phenotype

Degeneration of anterior horn cells [hp:0002398]
type: SIO_010056
comment: Phenotype [hp:0002398] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Degeneration of anterior horn cells
in dataset: phenotype

Confetti-like hypopigmented macules [hp:0007449]
type: SIO_010056
comment: Phenotype [hp:0007449] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Confetti-like hypopigmented macules
in dataset: phenotype

Caudal interpedicular narrowing [hp:0008457]
type: SIO_010056
comment: Phenotype [hp:0008457] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Caudal interpedicular narrowing
in dataset: phenotype

Arnold-Chiari malformation [hp:0002308]
type: SIO_010056
comment: Phenotype [hp:0002308] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Arnold-Chiari malformation
in dataset: phenotype

Retinal vascular malformation [hp:0007797]
type: SIO_010056
comment: Phenotype [hp:0007797] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal vascular malformation
in dataset: phenotype

Premaxillary Prominence [hp:0010759]
type: SIO_010056
comment: Phenotype [hp:0010759] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premaxillary Prominence
in dataset: phenotype

Complete heart block with narrow QRS complexes [hp:0005178]
type: SIO_010056
comment: Phenotype [hp:0005178] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Complete heart block with narrow QRS complexes
in dataset: phenotype

Cystic renal dysplasia [hp:0000800]
type: SIO_010056
comment: Phenotype [hp:0000800] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cystic renal dysplasia
in dataset: phenotype

Abnormal ossification of hand bones [hp:0005921]
type: SIO_010056
comment: Phenotype [hp:0005921] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal ossification of hand bones
in dataset: phenotype

Spastic gait [hp:0002064]
type: SIO_010056
comment: Phenotype [hp:0002064] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spastic gait
in dataset: phenotype

Mitral valve calcification [hp:0004382]
type: SIO_010056
comment: Phenotype [hp:0004382] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mitral valve calcification
in dataset: phenotype

Elongated sella turcica [hp:0005463]
type: SIO_010056
comment: Phenotype [hp:0005463] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elongated sella turcica
in dataset: phenotype

Pigmentary retinal deposits [hp:0007702]
type: SIO_010056
comment: Phenotype [hp:0007702] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pigmentary retinal deposits
in dataset: phenotype

Sparse scalp hair [hp:0002209]
type: SIO_010056
comment: Phenotype [hp:0002209] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sparse scalp hair
in dataset: phenotype

Fundus atrophy [hp:0001099]
type: SIO_010056
comment: Phenotype [hp:0001099] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Fundus atrophy
in dataset: phenotype

Sparse eyebrow [hp:0000535]
type: SIO_010056
comment: Phenotype [hp:0000535] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sparse eyebrow
in dataset: phenotype

Breast aplasia [hp:0100783]
type: SIO_010056
comment: Phenotype [hp:0100783] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Breast aplasia
in dataset: phenotype

Brushfield spots [hp:0001088]
type: SIO_010056
comment: Phenotype [hp:0001088] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Brushfield spots
in dataset: phenotype

Megalencephaly [hp:0001355]
type: SIO_010056
comment: Phenotype [hp:0001355] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Megalencephaly
in dataset: phenotype

Impulsivity [hp:0100710]
type: SIO_010056
comment: Phenotype [hp:0100710] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impulsivity
in dataset: phenotype

Postaxial polysyndactyly of foot [hp:0005817]
type: SIO_010056
comment: Phenotype [hp:0005817] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Postaxial polysyndactyly of foot
in dataset: phenotype

Broad jaw [hp:0012802]
type: SIO_010056
comment: Phenotype [hp:0012802] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad jaw
in dataset: phenotype

Abnormality of the globus pallidus [hp:0002453]
type: SIO_010056
comment: Phenotype [hp:0002453] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the globus pallidus
in dataset: phenotype

Premature loss of teeth [hp:0006480]
type: SIO_010056
comment: Phenotype [hp:0006480] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Premature loss of teeth
in dataset: phenotype

Receptive language delay [hp:0010863]
type: SIO_010056
comment: Phenotype [hp:0010863] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Receptive language delay
in dataset: phenotype

Progressive congenital scoliosis [hp:0008458]
type: SIO_010056
comment: Phenotype [hp:0008458] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Progressive congenital scoliosis
in dataset: phenotype

Pigmentary retinal degeneration [hp:0001146]
type: SIO_010056
comment: Phenotype [hp:0001146] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pigmentary retinal degeneration
in dataset: phenotype

Flexion limitation of toes [hp:0008116]
type: SIO_010056
comment: Phenotype [hp:0008116] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flexion limitation of toes
in dataset: phenotype

Bilateral triphalangeal thumbs [hp:0005707]
type: SIO_010056
comment: Phenotype [hp:0005707] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral triphalangeal thumbs
in dataset: phenotype

Macroorchidism [hp:0000053]
type: SIO_010056
comment: Phenotype [hp:0000053] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macroorchidism
in dataset: phenotype

Proximal tubulopathy [hp:0000114]
type: SIO_010056
comment: Phenotype [hp:0000114] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Proximal tubulopathy
in dataset: phenotype

Abnormal delayed hypersensitivity skin test [hp:0002963]
type: SIO_010056
comment: Phenotype [hp:0002963] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal delayed hypersensitivity skin test
in dataset: phenotype

Short iliac bones [hp:0100866]
type: SIO_010056
comment: Phenotype [hp:0100866] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short iliac bones
in dataset: phenotype

Dysmetric saccades [hp:0000641]
type: SIO_010056
comment: Phenotype [hp:0000641] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysmetric saccades
in dataset: phenotype

Papilledema [hp:0001085]
type: SIO_010056
comment: Phenotype [hp:0001085] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Papilledema
in dataset: phenotype

Peripheral arteriovenous fistula [hp:0100784]
type: SIO_010056
comment: Phenotype [hp:0100784] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral arteriovenous fistula
in dataset: phenotype

Cranial asymmetry [hp:0000267]
type: SIO_010056
comment: Phenotype [hp:0000267] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cranial asymmetry
in dataset: phenotype

Frontal encephalocele [hp:0007330]
type: SIO_010056
comment: Phenotype [hp:0007330] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontal encephalocele
in dataset: phenotype

Plantar hyperkeratosis [hp:0007556]
type: SIO_010056
comment: Phenotype [hp:0007556] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Plantar hyperkeratosis
in dataset: phenotype

Pulmonary arteriovenous malformation [hp:0006548]
type: SIO_010056
comment: Phenotype [hp:0006548] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary arteriovenous malformation
in dataset: phenotype

Exaggerated cellular immune processes [hp:0005397]
type: SIO_010056
comment: Phenotype [hp:0005397] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exaggerated cellular immune processes
in dataset: phenotype

Pseudobulbar signs [hp:0002200]
type: SIO_010056
comment: Phenotype [hp:0002200] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pseudobulbar signs
in dataset: phenotype

Generalized tonic-clonic seizures [hp:0002069]
type: SIO_010056
comment: Phenotype [hp:0002069] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized tonic-clonic seizures
in dataset: phenotype

Postural tremor [hp:0002174]
type: SIO_010056
comment: Phenotype [hp:0002174] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Postural tremor
in dataset: phenotype

Bone marrow hypocellularity [hp:0005528]
type: SIO_010056
comment: Phenotype [hp:0005528] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bone marrow hypocellularity
in dataset: phenotype

Type A brachydactyly [hp:0009370]
type: SIO_010056
comment: Phenotype [hp:0009370] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Type A brachydactyly
in dataset: phenotype

Chronic rhinitis due to narrow nasal airway [hp:0004499]
type: SIO_010056
comment: Phenotype [hp:0004499] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic rhinitis due to narrow nasal airway
in dataset: phenotype

High iliac wings [hp:0008808]
type: SIO_010056
comment: Phenotype [hp:0008808] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: High iliac wings
in dataset: phenotype

Wide-cupped costochondral junctions [hp:0000910]
type: SIO_010056
comment: Phenotype [hp:0000910] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Wide-cupped costochondral junctions
in dataset: phenotype

Elevated serum acid phosphatase [hp:0003148]
type: SIO_010056
comment: Phenotype [hp:0003148] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated serum acid phosphatase
in dataset: phenotype

Flat nasal alae [hp:0010649]
type: SIO_010056
comment: Phenotype [hp:0010649] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flat nasal alae
in dataset: phenotype

Retinal exudate [hp:0001147]
type: SIO_010056
comment: Phenotype [hp:0001147] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Retinal exudate
in dataset: phenotype

Bifid distal phalanx of the thumb [hp:0009611]
type: SIO_010056
comment: Phenotype [hp:0009611] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid distal phalanx of the thumb
in dataset: phenotype

Shortening of the talar neck [hp:0008117]
type: SIO_010056
comment: Phenotype [hp:0008117] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shortening of the talar neck
in dataset: phenotype

Micropenis [hp:0000054]
type: SIO_010056
comment: Phenotype [hp:0000054] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Micropenis
in dataset: phenotype

Acetabular dysplasia [hp:0008807]
type: SIO_010056
comment: Phenotype [hp:0008807] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acetabular dysplasia
in dataset: phenotype

Broad ischia [hp:0100865]
type: SIO_010056
comment: Phenotype [hp:0100865] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad ischia
in dataset: phenotype

Dolichocephaly [hp:0000268]
type: SIO_010056
comment: Phenotype [hp:0000268] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dolichocephaly
in dataset: phenotype

Keratoconjunctivitis sicca [hp:0001097]
type: SIO_010056
comment: Phenotype [hp:0001097] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Keratoconjunctivitis sicca
in dataset: phenotype

Red-green dyschromatopsia [hp:0000642]
type: SIO_010056
comment: Phenotype [hp:0000642] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Red-green dyschromatopsia
in dataset: phenotype

Insomnia [hp:0100785]
type: SIO_010056
comment: Phenotype [hp:0100785] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Insomnia
in dataset: phenotype

Dextrocardia [hp:0001651]
type: SIO_010056
comment: Phenotype [hp:0001651] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dextrocardia
in dataset: phenotype

Duodenal adenocarcinoma [hp:0006771]
type: SIO_010056
comment: Phenotype [hp:0006771] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Duodenal adenocarcinoma
in dataset: phenotype

Cutaneous syndactyly between fingers 2 and 5 [hp:0005650]
type: SIO_010056
comment: Phenotype [hp:0005650] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cutaneous syndactyly between fingers 2 and 5
in dataset: phenotype

Megaloblastic anemia [hp:0001889]
type: SIO_010056
comment: Phenotype [hp:0001889] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Megaloblastic anemia
in dataset: phenotype

Unilateral primary pulmonary dysgenesis [hp:0006549]
type: SIO_010056
comment: Phenotype [hp:0006549] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Unilateral primary pulmonary dysgenesis
in dataset: phenotype

Dermal translucency [hp:0010648]
type: SIO_010056
comment: Phenotype [hp:0010648] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dermal translucency
in dataset: phenotype

Flat glenoid fossa [hp:0000911]
type: SIO_010056
comment: Phenotype [hp:0000911] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flat glenoid fossa
in dataset: phenotype

Hyperuricosuria [hp:0003149]
type: SIO_010056
comment: Phenotype [hp:0003149] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperuricosuria
in dataset: phenotype

Broad fingertip [hp:0011300]
type: SIO_010056
comment: Phenotype [hp:0011300] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad fingertip
in dataset: phenotype

Flat occiput [hp:0005469]
type: SIO_010056
comment: Phenotype [hp:0005469] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Flat occiput
in dataset: phenotype

Increased urinary urate [hp:0012611]
type: SIO_010056
comment: Phenotype [hp:0012611] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased urinary urate
in dataset: phenotype

2-3 toe cutaneous syndactyly [hp:0005709]
type: SIO_010056
comment: Phenotype [hp:0005709] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: 2-3 toe cutaneous syndactyly
in dataset: phenotype

Perineal hypospadias [hp:0000051]
type: SIO_010056
comment: Phenotype [hp:0000051] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Perineal hypospadias
in dataset: phenotype

Generalized muscle hypertrophy [hp:0003720]
type: SIO_010056
comment: Phenotype [hp:0003720] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Generalized muscle hypertrophy
in dataset: phenotype

Absence of Lutheran antigen on erythrocytes [hp:0010971]
type: SIO_010056
comment: Phenotype [hp:0010971] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absence of Lutheran antigen on erythrocytes
in dataset: phenotype

Orbital cyst [hp:0001144]
type: SIO_010056
comment: Phenotype [hp:0001144] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Orbital cyst
in dataset: phenotype

Dysgammaglobulinemia [hp:0002961]
type: SIO_010056
comment: Phenotype [hp:0002961] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysgammaglobulinemia
in dataset: phenotype

Aortic valve stenosis [hp:0001650]
type: SIO_010056
comment: Phenotype [hp:0001650] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aortic valve stenosis
in dataset: phenotype

Hemifacial seizures [hp:0007332]
type: SIO_010056
comment: Phenotype [hp:0007332] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemifacial seizures
in dataset: phenotype

Enlarged labia minora [hp:0008683]
type: SIO_010056
comment: Phenotype [hp:0008683] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Enlarged labia minora
in dataset: phenotype

Blepharospasm [hp:0000643]
type: SIO_010056
comment: Phenotype [hp:0000643] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Blepharospasm
in dataset: phenotype

Ectopia lentis [hp:0001083]
type: SIO_010056
comment: Phenotype [hp:0001083] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ectopia lentis
in dataset: phenotype

Mastoiditis [hp:0000265]
type: SIO_010056
comment: Phenotype [hp:0000265] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mastoiditis
in dataset: phenotype

Nephropathy [hp:0000112]
type: SIO_010056
comment: Phenotype [hp:0000112] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Nephropathy
in dataset: phenotype

Keratoconjunctivitis [hp:0001096]
type: SIO_010056
comment: Phenotype [hp:0001096] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Keratoconjunctivitis
in dataset: phenotype

Lymphopenia [hp:0001888]
type: SIO_010056
comment: Phenotype [hp:0001888] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lymphopenia
in dataset: phenotype

Subretinal exudate [hp:0011532]
type: SIO_010056
comment: Phenotype [hp:0011532] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Subretinal exudate
in dataset: phenotype

Renal angiomyolipoma [hp:0006772]
type: SIO_010056
comment: Phenotype [hp:0006772] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal angiomyolipoma
in dataset: phenotype

Cutaneous melanoma [hp:0012056]
type: SIO_010056
comment: Phenotype [hp:0012056] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cutaneous melanoma
in dataset: phenotype

Smooth philtrum [hp:0000319]
type: SIO_010056
comment: Phenotype [hp:0000319] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Smooth philtrum
in dataset: phenotype

Postural instability [hp:0002172]
type: SIO_010056
comment: Phenotype [hp:0002172] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Postural instability
in dataset: phenotype

Bradykinesia [hp:0002067]
type: SIO_010056
comment: Phenotype [hp:0002067] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bradykinesia
in dataset: phenotype

Peripheral pulmonary vessel aplasia [hp:0005316]
type: SIO_010056
comment: Phenotype [hp:0005316] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral pulmonary vessel aplasia
in dataset: phenotype

Localized epidermolytic hyperkeratosis [hp:0007559]
type: SIO_010056
comment: Phenotype [hp:0007559] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Localized epidermolytic hyperkeratosis
in dataset: phenotype

Triangular shaped middle phalanx of the 2nd finger [hp:0009575]
type: SIO_010056
comment: Phenotype [hp:0009575] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular shaped middle phalanx of the 2nd finger
in dataset: phenotype

Chorioretinopathy [hp:0001145]
type: SIO_010056
comment: Phenotype [hp:0001145] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chorioretinopathy
in dataset: phenotype

Portal vein thrombosis [hp:0030242]
type: SIO_010056
comment: Phenotype [hp:0030242] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Portal vein thrombosis
in dataset: phenotype

Anemia of inadequate production [hp:0010972]
type: SIO_010056
comment: Phenotype [hp:0010972] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anemia of inadequate production
in dataset: phenotype

Polycystic kidney dysplasia [hp:0000113]
type: SIO_010056
comment: Phenotype [hp:0000113] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Polycystic kidney dysplasia
in dataset: phenotype

Autoimmunity [hp:0002960]
type: SIO_010056
comment: Phenotype [hp:0002960] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Autoimmunity
in dataset: phenotype

Corneal arcus [hp:0001084]
type: SIO_010056
comment: Phenotype [hp:0001084] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Corneal arcus
in dataset: phenotype

Hypoplasia of the frontal lobes [hp:0007333]
type: SIO_010056
comment: Phenotype [hp:0007333] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the frontal lobes
in dataset: phenotype

Prostate neoplasm [hp:0100787]
type: SIO_010056
comment: Phenotype [hp:0100787] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prostate neoplasm
in dataset: phenotype

Hypertensive retinopathy [hp:0001095]
type: SIO_010056
comment: Phenotype [hp:0001095] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertensive retinopathy
in dataset: phenotype

Deformed tarsal bones [hp:0008119]
type: SIO_010056
comment: Phenotype [hp:0008119] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Deformed tarsal bones
in dataset: phenotype

Duodenal stenosis [hp:0100867]
type: SIO_010056
comment: Phenotype [hp:0100867] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Duodenal stenosis
in dataset: phenotype

Developmental stagnation at onset of seizures [hp:0006834]
type: SIO_010056
comment: Phenotype [hp:0006834] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Developmental stagnation at onset of seizures
in dataset: phenotype

Hypoglycemic seizures [hp:0002173]
type: SIO_010056
comment: Phenotype [hp:0002173] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoglycemic seizures
in dataset: phenotype

Increased pulmonary vascular resistance [hp:0005317]
type: SIO_010056
comment: Phenotype [hp:0005317] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased pulmonary vascular resistance
in dataset: phenotype

Bilateral elbow dislocations [hp:0005021]
type: SIO_010056
comment: Phenotype [hp:0005021] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral elbow dislocations
in dataset: phenotype

Frontal open bite [hp:0200094]
type: SIO_010056
comment: Phenotype [hp:0200094] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Frontal open bite
in dataset: phenotype

Iridocyclitis [hp:0001094]
type: SIO_010056
comment: Phenotype [hp:0001094] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Iridocyclitis
in dataset: phenotype

Abnormal subcutaneous fat tissue distribution [hp:0007552]
type: SIO_010056
comment: Phenotype [hp:0007552] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal subcutaneous fat tissue distribution
in dataset: phenotype

Cardiac rhabdomyoma [hp:0009729]
type: SIO_010056
comment: Phenotype [hp:0009729] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cardiac rhabdomyoma
in dataset: phenotype

EEG with polyspike wave complexes [hp:0002392]
type: SIO_010056
comment: Phenotype [hp:0002392] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: EEG with polyspike wave complexes
in dataset: phenotype

Chronic metabolic acidosis [hp:0001996]
type: SIO_010056
comment: Phenotype [hp:0001996] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic metabolic acidosis
in dataset: phenotype

Cholelithiasis [hp:0001081]
type: SIO_010056
comment: Phenotype [hp:0001081] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cholelithiasis
in dataset: phenotype

Neck flexor weakness [hp:0003722]
type: SIO_010056
comment: Phenotype [hp:0003722] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neck flexor weakness
in dataset: phenotype

Oxycephaly [hp:0000263]
type: SIO_010056
comment: Phenotype [hp:0000263] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oxycephaly
in dataset: phenotype

Hypoplasia of deltoid muscle [hp:0030241]
type: SIO_010056
comment: Phenotype [hp:0030241] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of deltoid muscle
in dataset: phenotype

Prolactin excess [hp:0000870]
type: SIO_010056
comment: Phenotype [hp:0000870] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Prolactin excess
in dataset: phenotype

Broad femoral head [hp:0008804]
type: SIO_010056
comment: Phenotype [hp:0008804] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Broad femoral head
in dataset: phenotype

Anterior open bite [hp:0200095]
type: SIO_010056
comment: Phenotype [hp:0200095] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior open bite
in dataset: phenotype

Dyschromatopsia [hp:0007641]
type: SIO_010056
comment: Phenotype [hp:0007641] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dyschromatopsia
in dataset: phenotype

Aplasia/Hypoplasia of the lens [hp:0008063]
type: SIO_010056
comment: Phenotype [hp:0008063] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the lens
in dataset: phenotype

Macrocytic hemolytic disease [hp:0005524]
type: SIO_010056
comment: Phenotype [hp:0005524] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macrocytic hemolytic disease
in dataset: phenotype

Intracranial hemorrhage [hp:0002170]
type: SIO_010056
comment: Phenotype [hp:0002170] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intracranial hemorrhage
in dataset: phenotype

Anasarca [hp:0012050]
type: SIO_010056
comment: Phenotype [hp:0012050] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anasarca
in dataset: phenotype

Biliary tract abnormality [hp:0001080]
type: SIO_010056
comment: Phenotype [hp:0001080] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Biliary tract abnormality
in dataset: phenotype

Pulmonary embolism [hp:0002204]
type: SIO_010056
comment: Phenotype [hp:0002204] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary embolism
in dataset: phenotype

Ulnar bowing [hp:0003031]
type: SIO_010056
comment: Phenotype [hp:0003031] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ulnar bowing
in dataset: phenotype

Osteomalacia [hp:0002749]
type: SIO_010056
comment: Phenotype [hp:0002749] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Osteomalacia
in dataset: phenotype

Facial myokymia [hp:0000317]
type: SIO_010056
comment: Phenotype [hp:0000317] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Facial myokymia
in dataset: phenotype

Large vessel vasculitis [hp:0005310]
type: SIO_010056
comment: Phenotype [hp:0005310] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large vessel vasculitis
in dataset: phenotype

Toe extensor amyotrophy [hp:0011916]
type: SIO_010056
comment: Phenotype [hp:0011916] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Toe extensor amyotrophy
in dataset: phenotype

Protanomaly [hp:0200018]
type: SIO_010056
comment: Phenotype [hp:0200018] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Protanomaly
in dataset: phenotype

Increased serum serotonin [hp:0003144]
type: SIO_010056
comment: Phenotype [hp:0003144] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Increased serum serotonin
in dataset: phenotype

Optic nerve dysplasia [hp:0001093]
type: SIO_010056
comment: Phenotype [hp:0001093] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Optic nerve dysplasia
in dataset: phenotype

Torus palatinus [hp:0100789]
type: SIO_010056
comment: Phenotype [hp:0100789] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Torus palatinus
in dataset: phenotype

Patent foramen ovale [hp:0001655]
type: SIO_010056
comment: Phenotype [hp:0001655] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Patent foramen ovale
in dataset: phenotype

Abnormality of the mastoid [hp:0000264]
type: SIO_010056
comment: Phenotype [hp:0000264] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the mastoid
in dataset: phenotype

Cholecystitis [hp:0001082]
type: SIO_010056
comment: Phenotype [hp:0001082] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cholecystitis
in dataset: phenotype

Gout [hp:0001997]
type: SIO_010056
comment: Phenotype [hp:0001997] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gout
in dataset: phenotype

Congenital symmetrical palmoplantar keratosis [hp:0007553]
type: SIO_010056
comment: Phenotype [hp:0007553] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital symmetrical palmoplantar keratosis
in dataset: phenotype

Multiple plantar creases [hp:0008113]
type: SIO_010056
comment: Phenotype [hp:0008113] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple plantar creases
in dataset: phenotype

Hypoplastic male external genitalia [hp:0000050]
type: SIO_010056
comment: Phenotype [hp:0000050] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic male external genitalia
in dataset: phenotype

Narrow sacroiliac notch [hp:0008803]
type: SIO_010056
comment: Phenotype [hp:0008803] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Narrow sacroiliac notch
in dataset: phenotype

Dysautonomia [hp:0002459]
type: SIO_010056
comment: Phenotype [hp:0002459] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dysautonomia
in dataset: phenotype

Midnasal stenosis [hp:0010644]
type: SIO_010056
comment: Phenotype [hp:0010644] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Midnasal stenosis
in dataset: phenotype

Triangular-shaped open mouth [hp:0200096]
type: SIO_010056
comment: Phenotype [hp:0200096] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Triangular-shaped open mouth
in dataset: phenotype

Chronic hemolytic anemia [hp:0004870]
type: SIO_010056
comment: Phenotype [hp:0004870] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic hemolytic anemia
in dataset: phenotype

Abnormality of immune system physiology [hp:0010978]
type: SIO_010056
comment: Phenotype [hp:0010978] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of immune system physiology
in dataset: phenotype

Spontaneous hemolytic crises [hp:0005525]
type: SIO_010056
comment: Phenotype [hp:0005525] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spontaneous hemolytic crises
in dataset: phenotype

Pseudoepiphysis of the thumb [hp:0009693]
type: SIO_010056
comment: Phenotype [hp:0009693] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pseudoepiphysis of the thumb
in dataset: phenotype

Reactive hypoglycemia [hp:0012051]
type: SIO_010056
comment: Phenotype [hp:0012051] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reactive hypoglycemia
in dataset: phenotype

Gliosis [hp:0002171]
type: SIO_010056
comment: Phenotype [hp:0002171] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Gliosis
in dataset: phenotype

Short palm [hp:0004279]
type: SIO_010056
comment: Phenotype [hp:0004279] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short palm
in dataset: phenotype

Congenital stationary night blindness [hp:0007642]
type: SIO_010056
comment: Phenotype [hp:0007642] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Congenital stationary night blindness
in dataset: phenotype

Amblyopia [hp:0000646]
type: SIO_010056
comment: Phenotype [hp:0000646] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Amblyopia
in dataset: phenotype

Rickets [hp:0002748]
type: SIO_010056
comment: Phenotype [hp:0002748] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Rickets
in dataset: phenotype

Decreased adenosylcobalamin [hp:0003145]
type: SIO_010056
comment: Phenotype [hp:0003145] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased adenosylcobalamin
in dataset: phenotype

Left atrial isomerism [hp:0011537]
type: SIO_010056
comment: Phenotype [hp:0011537] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Left atrial isomerism
in dataset: phenotype

Palmar telangiectasia [hp:0100869]
type: SIO_010056
comment: Phenotype [hp:0100869] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Palmar telangiectasia
in dataset: phenotype

Agenesis of pulmonary vessels [hp:0005311]
type: SIO_010056
comment: Phenotype [hp:0005311] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Agenesis of pulmonary vessels
in dataset: phenotype

Respiratory paralysis [hp:0002203]
type: SIO_010056
comment: Phenotype [hp:0002203] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Respiratory paralysis
in dataset: phenotype

Self-injurious behavior [hp:0100716]
type: SIO_010056
comment: Phenotype [hp:0100716] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Self-injurious behavior
in dataset: phenotype

Abnormality of the genitourinary system [hp:0000119]
type: SIO_010056
comment: Phenotype [hp:0000119] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the genitourinary system
in dataset: phenotype

Hypertelorism [hp:0000316]
type: SIO_010056
comment: Phenotype [hp:0000316] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypertelorism
in dataset: phenotype

Neonatal hypoglycemia [hp:0001998]
type: SIO_010056
comment: Phenotype [hp:0001998] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Neonatal hypoglycemia
in dataset: phenotype

Spinal arteriovenous malformation [hp:0002390]
type: SIO_010056
comment: Phenotype [hp:0002390] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Spinal arteriovenous malformation
in dataset: phenotype

Recurrent opportunistic infections [hp:0005390]
type: SIO_010056
comment: Phenotype [hp:0005390] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Recurrent opportunistic infections
in dataset: phenotype

Hypoplasia of the prostate [hp:0008687]
type: SIO_010056
comment: Phenotype [hp:0008687] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplasia of the prostate
in dataset: phenotype

Abnormality of the heart valves [hp:0001654]
type: SIO_010056
comment: Phenotype [hp:0001654] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of the heart valves
in dataset: phenotype

Ulcerative colitis [hp:0100279]
type: SIO_010056
comment: Phenotype [hp:0100279] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ulcerative colitis
in dataset: phenotype

Achromatic retinal patches [hp:0009727]
type: SIO_010056
comment: Phenotype [hp:0009727] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Achromatic retinal patches
in dataset: phenotype

Absent lacrimal punctum [hp:0001092]
type: SIO_010056
comment: Phenotype [hp:0001092] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent lacrimal punctum
in dataset: phenotype

Metatarsal diaphyseal endosteal sclerosis [hp:0008114]
type: SIO_010056
comment: Phenotype [hp:0008114] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Metatarsal diaphyseal endosteal sclerosis
in dataset: phenotype

Complete heart block with broad RS complexes [hp:0005170]
type: SIO_010056
comment: Phenotype [hp:0005170] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Complete heart block with broad RS complexes
in dataset: phenotype

Cleft mandible [hp:0010752]
type: SIO_010056
comment: Phenotype [hp:0010752] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Cleft mandible
in dataset: phenotype

Hemiplegia [hp:0002301]
type: SIO_010056
comment: Phenotype [hp:0002301] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hemiplegia
in dataset: phenotype

Abnormal blistering of the skin [hp:0008066]
type: SIO_010056
comment: Phenotype [hp:0008066] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal blistering of the skin
in dataset: phenotype

Shoulder girdle muscle atrophy [hp:0003724]
type: SIO_010056
comment: Phenotype [hp:0003724] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Shoulder girdle muscle atrophy
in dataset: phenotype

Abnormal anterior horn cell morphology [hp:0006802]
type: SIO_010056
comment: Phenotype [hp:0006802] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal anterior horn cell morphology
in dataset: phenotype

Peripheral traction retinal detachment [hp:0007643]
type: SIO_010056
comment: Phenotype [hp:0007643] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral traction retinal detachment
in dataset: phenotype

Aplasia/Hypoplasia of the skin [hp:0008065]
type: SIO_010056
comment: Phenotype [hp:0008065] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aplasia/Hypoplasia of the skin
in dataset: phenotype

Multiple digital exostoses [hp:0005655]
type: SIO_010056
comment: Phenotype [hp:0005655] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Multiple digital exostoses
in dataset: phenotype

Oral mucosal blisters [hp:0200097]
type: SIO_010056
comment: Phenotype [hp:0200097] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Oral mucosal blisters
in dataset: phenotype

Onychauxis [hp:0012542]
type: SIO_010056
comment: Phenotype [hp:0012542] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Onychauxis
in dataset: phenotype

Hypocholesterolemia [hp:0003146]
type: SIO_010056
comment: Phenotype [hp:0003146] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypocholesterolemia
in dataset: phenotype

Pulmonary aterial intimal fibrosis [hp:0005312]
type: SIO_010056
comment: Phenotype [hp:0005312] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pulmonary aterial intimal fibrosis
in dataset: phenotype

Pleural effusion [hp:0002202]
type: SIO_010056
comment: Phenotype [hp:0002202] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Pleural effusion
in dataset: phenotype

Right atrial isomerism [hp:0011536]
type: SIO_010056
comment: Phenotype [hp:0011536] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Right atrial isomerism
in dataset: phenotype

Respiratory insufficiency due to muscle weakness [hp:0002747]
type: SIO_010056
comment: Phenotype [hp:0002747] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Respiratory insufficiency due to muscle weakness
in dataset: phenotype

Acrokeratosis [hp:0200016]
type: SIO_010056
comment: Phenotype [hp:0200016] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Acrokeratosis
in dataset: phenotype

Lens coloboma [hp:0100719]
type: SIO_010056
comment: Phenotype [hp:0100719] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lens coloboma
in dataset: phenotype

Sclerocornea [hp:0000647]
type: SIO_010056
comment: Phenotype [hp:0000647] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Sclerocornea
in dataset: phenotype

Mitral regurgitation [hp:0001653]
type: SIO_010056
comment: Phenotype [hp:0001653] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mitral regurgitation
in dataset: phenotype

Renal phosphate wasting [hp:0000117]
type: SIO_010056
comment: Phenotype [hp:0000117] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal phosphate wasting
in dataset: phenotype

Renal neoplasm [hp:0009726]
type: SIO_010056
comment: Phenotype [hp:0009726] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Renal neoplasm
in dataset: phenotype

Occipital neuralgia [hp:0012318]
type: SIO_010056
comment: Phenotype [hp:0012318] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Occipital neuralgia
in dataset: phenotype

Lattice corneal dystrophy [hp:0001149]
type: SIO_010056
comment: Phenotype [hp:0001149] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Lattice corneal dystrophy
in dataset: phenotype

Chin dimple [hp:0010751]
type: SIO_010056
comment: Phenotype [hp:0010751] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chin dimple
in dataset: phenotype

Mutism [hp:0002300]
type: SIO_010056
comment: Phenotype [hp:0002300] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Mutism
in dataset: phenotype

Firm muscles [hp:0003725]
type: SIO_010056
comment: Phenotype [hp:0003725] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Firm muscles
in dataset: phenotype

Turricephaly [hp:0000262]
type: SIO_010056
comment: Phenotype [hp:0000262] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Turricephaly
in dataset: phenotype

Absent skin pigmentation [hp:0200098]
type: SIO_010056
comment: Phenotype [hp:0200098] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Absent skin pigmentation
in dataset: phenotype

Ichthyosis [hp:0008064]
type: SIO_010056
comment: Phenotype [hp:0008064] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ichthyosis
in dataset: phenotype

Positional foot deformity [hp:0005656]
type: SIO_010056
comment: Phenotype [hp:0005656] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Positional foot deformity
in dataset: phenotype

B lymphocytopenia [hp:0010976]
type: SIO_010056
comment: Phenotype [hp:0010976] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: B lymphocytopenia
in dataset: phenotype

Reduced kininogen activity [hp:0005527]
type: SIO_010056
comment: Phenotype [hp:0005527] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Reduced kininogen activity
in dataset: phenotype

Hyperactive deep tendon reflexes [hp:0006801]
type: SIO_010056
comment: Phenotype [hp:0006801] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hyperactive deep tendon reflexes
in dataset: phenotype

Short 5th toe [hp:0011917]
type: SIO_010056
comment: Phenotype [hp:0011917] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short 5th toe
in dataset: phenotype

Diaphyseal sclerosis [hp:0003034]
type: SIO_010056
comment: Phenotype [hp:0003034] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diaphyseal sclerosis
in dataset: phenotype

Large eyes [hp:0001090]
type: SIO_010056
comment: Phenotype [hp:0001090] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Large eyes
in dataset: phenotype

Uterine rupture [hp:0100718]
type: SIO_010056
comment: Phenotype [hp:0100718] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Uterine rupture
in dataset: phenotype

Abnormal facial shape [hp:0001999]
type: SIO_010056
comment: Phenotype [hp:0001999] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormal facial shape
in dataset: phenotype

Optic atrophy [hp:0000648]
type: SIO_010056
comment: Phenotype [hp:0000648] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Optic atrophy
in dataset: phenotype

Peripheral nerve compression [hp:0003406]
type: SIO_010056
comment: Phenotype [hp:0003406] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral nerve compression
in dataset: phenotype

Aortic regurgitation [hp:0001659]
type: SIO_010056
comment: Phenotype [hp:0001659] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Aortic regurgitation
in dataset: phenotype

Elevated mean arterial pressure [hp:0004972]
type: SIO_010056
comment: Phenotype [hp:0004972] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Elevated mean arterial pressure
in dataset: phenotype

Short metacarpals with rounded proximal ends [hp:0006161]
type: SIO_010056
comment: Phenotype [hp:0006161] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Short metacarpals with rounded proximal ends
in dataset: phenotype

Exercise-induced lactic acidemia [hp:0004901]
type: SIO_010056
comment: Phenotype [hp:0004901] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Exercise-induced lactic acidemia
in dataset: phenotype

Anterior rib cupping [hp:0000907]
type: SIO_010056
comment: Phenotype [hp:0000907] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Anterior rib cupping
in dataset: phenotype

Chronic oral candidiasis [hp:0009098]
type: SIO_010056
comment: Phenotype [hp:0009098] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Chronic oral candidiasis
in dataset: phenotype

Decreased activity of mitochondrial complex IV [hp:0008347]
type: SIO_010056
comment: Phenotype [hp:0008347] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Decreased activity of mitochondrial complex IV
in dataset: phenotype

Slender toe [hp:0011308]
type: SIO_010056
comment: Phenotype [hp:0011308] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Slender toe
in dataset: phenotype

Diabetes insipidus [hp:0000873]
type: SIO_010056
comment: Phenotype [hp:0000873] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diabetes insipidus
in dataset: phenotype

Malar flattening [hp:0000272]
type: SIO_010056
comment: Phenotype [hp:0000272] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Malar flattening
in dataset: phenotype

Bilateral cleft lip and palate [hp:0002744]
type: SIO_010056
comment: Phenotype [hp:0002744] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bilateral cleft lip and palate
in dataset: phenotype

Bifid ureter [hp:0030037]
type: SIO_010056
comment: Phenotype [hp:0030037] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Bifid ureter
in dataset: phenotype

Impaired horizontal smooth pursuit [hp:0001151]
type: SIO_010056
comment: Phenotype [hp:0001151] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Impaired horizontal smooth pursuit
in dataset: phenotype

Abnormality of leukocytes [hp:0001881]
type: SIO_010056
comment: Phenotype [hp:0001881] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Abnormality of leukocytes
in dataset: phenotype

Intestinal duplication [hp:0100668]
type: SIO_010056
comment: Phenotype [hp:0100668] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Intestinal duplication
in dataset: phenotype

Primary hypercorticolism [hp:0001579]
type: SIO_010056
comment: Phenotype [hp:0001579] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Primary hypercorticolism
in dataset: phenotype

Hypoplastic toenails [hp:0001800]
type: SIO_010056
comment: Phenotype [hp:0001800] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hypoplastic toenails
in dataset: phenotype

Ketoacidosis [hp:0001993]
type: SIO_010056
comment: Phenotype [hp:0001993] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Ketoacidosis
in dataset: phenotype

Hepatosplenomegaly [hp:0001433]
type: SIO_010056
comment: Phenotype [hp:0001433] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Hepatosplenomegaly
in dataset: phenotype

Histiocytoma [hp:0012315]
type: SIO_010056
comment: Phenotype [hp:0012315] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Histiocytoma
in dataset: phenotype

Diffuse axonal swelling [hp:0003405]
type: SIO_010056
comment: Phenotype [hp:0003405] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Diffuse axonal swelling
in dataset: phenotype

Dentinogenesis imperfecta [hp:0000703]
type: SIO_010056
comment: Phenotype [hp:0000703] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Dentinogenesis imperfecta
in dataset: phenotype

Median cleft palate [hp:0009099]
type: SIO_010056
comment: Phenotype [hp:0009099] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Median cleft palate
in dataset: phenotype

Severe lactic acidosis [hp:0004900]
type: SIO_010056
comment: Phenotype [hp:0004900] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Severe lactic acidosis
in dataset: phenotype

Widened proximal tibial metaphyses [hp:0005028]
type: SIO_010056
comment: Phenotype [hp:0005028] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Widened proximal tibial metaphyses
in dataset: phenotype

Macrocytic dyserythropoietic anemia [hp:0005532]
type: SIO_010056
comment: Phenotype [hp:0005532] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Macrocytic dyserythropoietic anemia
in dataset: phenotype

Soft tissue swelling of interphalangeal joints [hp:0006162]
type: SIO_010056
comment: Phenotype [hp:0006162] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Soft tissue swelling of interphalangeal joints
in dataset: phenotype

Peripheral retinal pigmentation abnormalities [hp:0200099]
type: SIO_010056
comment: Phenotype [hp:0200099] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Peripheral retinal pigmentation abnormalities
in dataset: phenotype

Refractory macrocytic anemia [hp:0004861]
type: SIO_010056
comment: Phenotype [hp:0004861] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
title: Refractory macrocytic anemia
in dataset: phenotype