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.

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.

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.
Congenital finger flexion contractures [hp:0005879]

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.

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.

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.
Type 1 muscle fiber predominance [hp:0003803]

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.
Irregular proximal tibial epiphyses [hp:0006456]

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.

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.

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.

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.
Premature fusion of phalangeal epiphyses [hp:0006140]
Premature fusion of phalangeal epiphyses

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.
Abnormal natural killer cell physiology [hp:0012177]

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.

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.

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.

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.

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.

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.
Abolished electroretinogram (ERG) [hp:0000550]

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.

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.

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.

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.
Recurrent Aspergillus infections [hp:0002724]

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.

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.
Pituitary growth hormone cell adenoma [hp:0011760]

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.

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.
Abnormality of the philtrum [hp:0000288]

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.
Corticospinal tract hypoplasia [hp:0007016]

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.

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.

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.

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.

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.

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.
Lower thoracic interpediculate narrowness [hp:0008470]
Lower thoracic interpediculate narrowness

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.
Cuboid-shaped vertebral bodies [hp:0004634]

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.
Clinodactyly of the 5th finger [hp:0004209]

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.

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.

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.

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.
Systemic lupus erythematosus [hp:0002725]

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.

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.
Impairment of fructose metabolism [hp:0011033]

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.
Increased hepatic glycogen content [hp:0006568]

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.
Ebstein's anomaly of the tricuspid valve [hp:0010316]
Ebstein's anomaly of the tricuspid valve

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.

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.

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.

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.
Reduced natural killer cell activity [hp:0012178]

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.

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.
Abnormality of color vision [hp:0000551]

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.
Ph-positive acute lymphoblastic leukemia [hp:0004848]
Ph-positive acute lymphoblastic leukemia

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.

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.

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.
Intestinal lymphangiectasia [hp:0002593]

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.
Increased facial adipose tissue [hp:0000287]

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.
Poor gross motor coordination [hp:0007015]

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.

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.
Delayed proximal femoral epiphyseal ossification [hp:0008828]
Delayed proximal femoral epiphyseal ossification

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.

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.
Abnormal metaphyseal trabeculation [hp:0005089]

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.

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.
Cervical vertebrae fusion (C5/C6) [hp:0004635]

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.

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.
Progressive calcification of costochondral cartilage [hp:0006600]
Progressive calcification of costochondral cartilage

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.

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.
Diffuse demyelination of the cerebral white matter [hp:0007162]
Diffuse demyelination of the cerebral white matter

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.

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.
Resistance to activated protein C [hp:0012175]

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.
Duplication of the proximal phalanx of the hallux [hp:0010093]
Duplication of the proximal phalanx of the hallux

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.
Attenuation of retinal blood vessels [hp:0007843]

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.

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.

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.

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.
Elevated systolic blood pressure [hp:0004421]

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.

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.

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.
Attention deficit hyperactivity disorder [hp:0007018]
Attention deficit hyperactivity disorder

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.

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.

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.
Recurrent abscess formation [hp:0002722]

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.

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.
Abnormal finger flexion creases [hp:0006143]

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.

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.
Functional respiratory abnormality [hp:0002795]

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.

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.
Absent/shortened outer dynein arms [hp:0200109]

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.

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.

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.
Delayed femoral head ossification [hp:0008829]

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.
Restricted large joint movement [hp:0005193]

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.

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.

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.

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.
Abnormality of iron homeostasis [hp:0011031]

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.
Cherry red spot of the macula [hp:0010729]

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.

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.

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.
Prominent protruding coccyx [hp:0008472]

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.
Abnormality of natural killer cells [hp:0012176]

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.

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.

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.
Cone-shaped epiphysis of the 1st metacarpal [hp:0010017]
Cone-shaped epiphysis of the 1st metacarpal

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.
Neoplasm of the oral cavity [hp:0100649]

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.

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.
Focal T2 hyperintense basal ganglia lesion [hp:0007183]
Focal T2 hyperintense basal ganglia lesion

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.

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.

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.

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.
Absence of bactericidal oxidative 'respiratory burst' in phagocytes [hp:0002723]
Absence of bactericidal oxidative 'respiratory burst' in phagocytes

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.
Supranuclear ophthalmoplegia [hp:0000623]

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.
Partial agenesis of the corpus callosum [hp:0001338]

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.

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.
Aplasia/Hypoplasia of the pancreas [hp:0100800]

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.

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.

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.
Narrow anterio-posterior vertebral body diameter [hp:0008473]
Narrow anterio-posterior vertebral body diameter

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.

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.

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.
Hernia of the abdominal wall [hp:0004299]

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.
Chronic mucocutaneous candidiasis [hp:0002728]

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.
3-Methylglutaconic aciduria [hp:0003535]

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.

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.

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.
Amyloid deposition in the vitreous humor [hp:0007841]
Amyloid deposition in the vitreous humor

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.
Reduced factor VIII activity [hp:0003125]

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.
High-frequency hearing impairment [hp:0005101]

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.
Biconcave flattened vertebrae [hp:0003321]

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.

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.
Abnormality of adipose tissue [hp:0009124]

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.

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.
Abnormal pattern of respiration [hp:0002793]

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.
Periventricular gray matter heterotopia [hp:0007165]

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.
Hyperplastic callus formation [hp:0030268]

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.
Abnormally low-pitched voice [hp:0010300]

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.

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.

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.

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.

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.

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.
Aplasia/Hypoplasia of the breasts [hp:0010311]

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.
Abdominal wall muscle weakness [hp:0009023]

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.

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.

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.
Reduced xanthine dehydrogenase activity [hp:0003534]

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.
Anterior beaking of thoracic vertebrae [hp:0004630]

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.
Coombs-positive hemolytic anemia [hp:0004844]

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.
Agenesis of mandibular central incisor [hp:0006355]

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.

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.

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.
Increased serum insulin-like growth factor 1 {comment="HPO:probinson"} [hp:0030269]
Increased serum insulin-like growth factor 1 {comment="HPO:probinson"}

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.

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.
Progressive flexion contractures [hp:0005876]

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.
Premature birth following premature rupture of fetal membranes [hp:0005100]
Premature birth following premature rupture of fetal membranes

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.

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.

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.

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.

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.
Palpitations (with pheochromocytoma) [hp:0001676]

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.

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.
Shortening of all proximal phalanges of the fingers [hp:0006144]
Shortening of all proximal phalanges of the fingers

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.
Increased CSF interferon alpha [hp:0009709]

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.

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.

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.

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.

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.
Severe combined immunodeficiency [hp:0004430]

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.
Abnormality of neuronal migration [hp:0002269]

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.

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.
Urinary bladder sphincter dysfunction [hp:0002839]

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.
Bony spicule pigmentary retinopathy [hp:0007737]

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.

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.
Delayed oxidation of acetaldehyde [hp:0003533]

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.

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.
Partial duplication of the distal phalanx of the hallux [hp:0010097]
Partial duplication of the distal phalanx of the hallux

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.
Recurrent Staphylococcus aureus infections [hp:0002726]
Recurrent Staphylococcus aureus infections

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.

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.
Delayed patellar ossification [hp:0006454]

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.
Calcification of the auricular cartilage [hp:0005103]
Calcification of the auricular cartilage

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.
Asymmetry of intraocular pressure [hp:0012633]

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.

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.
Decreased cervical spine flexion due to contractures of posterior cervical muscles [hp:0004631]
Decreased cervical spine flexion due to contractures of posterior cervical muscles

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.

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.
Decreased number of small peripheral myelinated nerve fibers [hp:0007249]
Decreased number of small peripheral myelinated nerve fibers

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.

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.

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.
Abnormality of the amniotic fluid [hp:0001560]

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.
Increased connective tissue [hp:0009025]

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.
Abnormality of the lymphatic system [hp:0100763]

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.
Tachycardia (with pheochromocytoma) [hp:0001673]

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.

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.

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.

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.

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.
Progressive fusion 2nd-5th pip joints [hp:0006147]

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.

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.

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.

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.
Prolonged bleeding after surgery [hp:0004846]

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.

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.

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.
Abnormality of the abdominal wall [hp:0004298]

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.

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.

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.

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.
Lateral displacement of the femoral head [hp:0006453]
Lateral displacement of the femoral head

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.
Cervical segmentation defect [hp:0004632]

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.

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.
Premature loss of permanent teeth [hp:0006357]

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.

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.
Low-molecular-weight proteinuria [hp:0003126]

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.
Neonatal breathing dysregulation [hp:0002790]

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.

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.

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.

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.

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.

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.

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.

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.
Nonspherocytic hemolytic anemia [hp:0001930]

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.
Hypoplasia of latissimus dorsi muscle [hp:0009026]

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.
Complete atrioventricular canal defect [hp:0001674]

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.

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.

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.

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.
Communicating hydrocephalus [hp:0001334]

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.

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.

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.
Foam cells with lamellar inclusion bodies [hp:0003609]
Foam cells with lamellar inclusion bodies

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.

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.

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.
Widely-spaced maxillary central incisors [hp:0001566]
Widely-spaced maxillary central incisors

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.
Aplasia of the proximal phalanges of the hand [hp:0010242]
Aplasia of the proximal phalanges of the hand

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.

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.
Abnormal hand bone ossification [hp:0010660]

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.
Abnormality of the cardiac septa [hp:0001671]

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.
Paraganglioma-related cranial nerve palsy [hp:0002377]
Paraganglioma-related cranial nerve palsy

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.
Type 1 and type 2 muscle fiber minicore regions [hp:0003787]
Type 1 and type 2 muscle fiber minicore regions

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.
Peripapillary chorioretinal atrophy [hp:0007950]

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.
Lipid accumulation in hepatocytes [hp:0006561]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Urinary bladder inflammation [hp:0100577]

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.

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.

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.
Hypoplastic vertebral bodies [hp:0008479]

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.

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.

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.
Hyperinsulinemic hypoglycemia [hp:0000825]

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.

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.
Small distal femoral epiphysis [hp:0012283]

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.

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.
Hypochromic microcytic anemia [hp:0004840]

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.
Peripheral axonal neuropathy [hp:0003477]

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.

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.
Intermittent lactic acidemia [hp:0004913]

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.

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.
Increased serum iduronate sulfatase activity [hp:0003538]
Increased serum iduronate sulfatase activity

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.

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.
Acral ulceration and osteomyelitis leading to autoamputation of the digits (feet) [hp:0001862]
Acral ulceration and osteomyelitis leading to autoamputation of the digits (feet)

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.

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.

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.

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.

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.
Autosomal dominant somatic cell mutation [hp:0001444]
Autosomal dominant somatic cell mutation

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.

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.

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.

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.

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.
Hyporeflexia of lower limbs [hp:0002600]

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.
Map-dot-fingerprint corneal dystrophy [hp:0007690]

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.
Poor fine motor coordination [hp:0007010]

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.
Minicore (multicore) myopathy [hp:0003789]

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.

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.

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.
Abnormality of the diencephalon [hp:0010662]

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.

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.
Malformation of the hepatic ductal plate [hp:0006563]
Malformation of the hepatic ductal plate

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.
Enlarged interphalangeal joints [hp:0006247]

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.

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.
Mandibular condyle hypoplasia [hp:0007628]

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.
Renal corticomedullary cysts [hp:0000108]

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.

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.

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.

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.

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.

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.

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.
Reduced factor XII activity [hp:0004841]

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.
Impairment of galactose metabolism [hp:0004915]

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.
Short proximal phalanx of finger [hp:0010241]

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.

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.
Autoimmune antibody positivity [hp:0030057]

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.

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.
Abnormality of thalamus morphology [hp:0010663]

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.
Asymmetric septal hypertrophy [hp:0001670]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Bilateral intracranial calcifications [hp:0005671]

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.

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.

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.
Persistent bleeding after trauma [hp:0001934]

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.
Decreased fumarate hydratase activity [hp:0003536]

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.

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.
Abnormality of the vertebral endplates [hp:0005106]

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.
Multiple mitochondrial DNA deletions [hp:0003689]

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.
Medial rotation of the medial malleolus [hp:0008132]

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.
Irregular sclerotic endplates [hp:0008476]

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.

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.
Synostosis involving bones of the fingers [hp:0009700]
Synostosis involving bones of the fingers

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.

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.

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.

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.

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.

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.
Externally rotated/abducted legs [hp:0003783]

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.
Cystic angiomatosis of bone [hp:0002833]

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.
Generalized distal tubular acidosis [hp:0004916]

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.
Perifollicular hyperkeratosis [hp:0007468]

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.

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.

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.

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.

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.
Intervertebral space narrowing [hp:0002945]

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.
Microangiopathic hemolytic anemia [hp:0001937]

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.
Decreased activity of cytochrome C oxidase in muscle tissue [hp:0003688]
Decreased activity of cytochrome C oxidase in muscle tissue

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.

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.
Abnormality of the respiratory system [hp:0002086]

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.
Abnormal hypothalamus morphology [hp:0012286]

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.
Increased hepatocellular lipid droplets [hp:0006565]

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.

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.

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.

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.
Decreased cervical spine mobility [hp:0004637]

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.
Distal tapering of metatarsals [hp:0008133]

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.

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.

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.

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.

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.
Hypoplastic sacral vertebrae [hp:0008475]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Ectopic ossification in ligament tissue [hp:0011989]

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.

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.
Centrally nucleated skeletal muscle fibers [hp:0003687]
Centrally nucleated skeletal muscle fibers

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.
Abnormality of the intervertebral disk [hp:0005108]

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.
Hypothalamic luteinizing hormone-releasing hormone deficiency [hp:0012287]
Hypothalamic luteinizing hormone-releasing hormone deficiency

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.

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.
Generalized morning stiffness [hp:0005197]

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.
Telangiectasia of extensor surfaces [hp:0007621]

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.

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.
Juvenile gastrointestinal polyposis [hp:0004784]

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.

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.

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.
Decreased CSF homovanillic acid (HVA) [hp:0003785]

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.
Anterior radial head dislocation [hp:0005084]

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.

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.
Abnormality of the thyroid gland [hp:0000820]

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.

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.
Elevated amniotic fluid alpha-fetoprotein [hp:0004639]
Elevated amniotic fluid alpha-fetoprotein

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.

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.
Irregular tarsal ossification [hp:0008134]

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.
Scheuermann-like vertebral changes [hp:0008478]

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.

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.

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.
4-Hydroxyphenylacetic aciduria [hp:0003607]

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.

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.

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.
Hyperchloremic metabolic acidosis [hp:0004918]

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.

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.
Abnormality of metabolism/homeostasis [hp:0001939]

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.

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.

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.
Multicentric ossification of proximal humeral epiphyses [hp:0004997]
Multicentric ossification of proximal humeral epiphyses

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.
Ectopic ossification in tendon tissue [hp:0011988]

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.

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.

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.

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.

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.
Limited knee flexion/extension [hp:0005085]

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.
Stiff interphalangeal joints [hp:0005198]

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.
Nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic) [hp:0003809]
Nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic)

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.
Small proximal tibial epiphyses [hp:0012284]

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.
Abnormal pupillary light reflex [hp:0007695]

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.
Palmoplantar hyperkeratosis [hp:0000972]

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.
Type 1 collagen overmodification [hp:0003784]

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.

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.
Poorly ossified cervical vertebrae [hp:0008477]

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.

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.

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.

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.
Submucous cleft hard palate [hp:0000176]

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.

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.

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.

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.
Ectopic ossification in muscle tissue [hp:0011987]

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.

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.

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.

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.
Pigmentation anomalies of sun-exposed skin [hp:0007623]
Pigmentation anomalies of sun-exposed skin

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.
Aplasia/Hypoplasia of the abdominal wall musculature [hp:0010318]
Aplasia/Hypoplasia of the abdominal wall musculature

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.
Aplasia of the abdominal wall musculature [hp:0005199]
Aplasia of the abdominal wall musculature

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.

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.
Neonatal cholestatic liver disease [hp:0006566]

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.

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.

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.
Retinal pigment epithelial atrophy [hp:0007698]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Pericentral retinitis pigmentosa [hp:0007947]

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.

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.

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.

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.
Abnormality of the male genitalia [hp:0010461]

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.
Absent proximal phalanx of thumb [hp:0009637]

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.

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.

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.

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.
Abnormality of the fifth metatarsal bone [hp:0008089]
Abnormality of the fifth metatarsal bone

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.

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.
Hemianopic blurring of vision [hp:0001125]

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.

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.

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.

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.
Abnormality of the vestibulocochlear nerve [hp:0009591]
Abnormality of the vestibulocochlear nerve

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.
Respiratory insufficiency due to defective ciliary clearance [hp:0200073]
Respiratory insufficiency due to defective ciliary clearance

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.

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.

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.

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.

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.
Unilateral narrow palpebral fissure [hp:0007946]

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.
Absent proximal finger flexion creases [hp:0006077]

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.

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.

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.
Short proximal phalanx of thumb [hp:0009638]

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.
Deposits immunoreactive to beta-amyloid protein [hp:0003791]
Deposits immunoreactive to beta-amyloid protein

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Abnormality of the autonomic nervous system [hp:0002270]
Abnormality of the autonomic nervous system

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.

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.

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.

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.

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.

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.

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.

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.
Wolff-Parkinson-White syndrome [hp:0001716]

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.

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.

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.
Cervical spine hypermobility [hp:0003318]

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.
Diaphoresis (with pheochromocytoma) [hp:0001011]

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.

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.
Honeycomb palmoplantar keratoderma [hp:0007465]

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.

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.
Enlarged epiphysis of the proximal phalanx of the 3rd finger [hp:0009349]
Enlarged epiphysis of the proximal phalanx of the 3rd finger

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.

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.
Ureteropelvic junction obstruction [hp:0000074]

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.
Bracket epiphysis of the middle phalanx of the 2nd finger [hp:0009514]
Bracket epiphysis of the middle phalanx of the 2nd finger

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.

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.
Peripheral vitreoretinal degeneration [hp:0200071]

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.
Late-onset proximal muscle weakness [hp:0003694]

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.

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.
Nonossified fifth metatarsal [hp:0008087]

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.

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.
Frontoparietal cortical dysplasia [hp:0006930]

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.

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.

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.
Hyperostosis cranialis interna [hp:0005890]

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.
Coronary artery calcification [hp:0001717]

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.
Intermittent microsaccadic pursuits [hp:0007944]

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.
Digital flexor tenosynovitis [hp:0012276]

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.
Abnormality of the cervical spine [hp:0003319]

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.
Midfrontal capillary hemangioma [hp:0007466]

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.
Asymmetric, linear skin defects [hp:0007398]

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.

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.

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.
Symmetrical, oval parietal bone defects [hp:0002695]

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.

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.

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.
Increased nuchal translucency [hp:0010880]

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.

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.

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.

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.

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.

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.
Fine, reticulate skin pigmentation [hp:0007617]

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.
Sensorineural hearing impairment [hp:0000407]

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.

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.
Generalized myoclonic seizures [hp:0002123]

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.

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.

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.

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.
Intermittent hyperpnea at rest [hp:0005941]

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.

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.

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.
Severe sensorineural hearing impairment [hp:0008625]

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.
Paresis of extensor muscles of the big toe [hp:0002601]
Paresis of extensor muscles of the big toe

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.

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.

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.

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.
Enlarged epiphysis of the middle phalanx of the 2nd finger [hp:0009516]
Enlarged epiphysis of the middle phalanx of the 2nd finger

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.

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.

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.

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.
Double outlet right ventricle [hp:0001719]

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.
Progressive sensorineural hearing impairment [hp:0000408]
Progressive sensorineural hearing impairment

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.
Epiphyseal deformities of tubular bones [hp:0003053]

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.

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.
Abnormality of the endocrine system [hp:0000818]

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.
Aplasia/Hypoplasia of the lungs [hp:0006703]

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.

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.

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.

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.

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.

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.
Pelvic girdle muscle atrophy [hp:0008988]

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.
Abnormal palmar dermatoglyphics [hp:0001018]

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.
Difficulty in tongue movements [hp:0000183]

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.

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.

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.
Clinodactyly of the 5th toe [hp:0001864]

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.

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.

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.

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.
Progressive macular scarring [hp:0007949]

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.
Episodic metabolic acidosis [hp:0004911]

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.

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.

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.

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.

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.

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.
Medial deviation of the foot [hp:0008082]

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.

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.

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.
Hypergonadotropic hypogonadism [hp:0000815]

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.
Abnormality of complement system [hp:0005339]

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.

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.

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.
Prominent superficial veins [hp:0001015]

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.
Abnormal lower motor neuron morphology [hp:0002366]

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.

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.

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.

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.
Abnormality of the genital system [hp:0000078]

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.

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.

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.

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.

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.

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.
Bicarbonate-wasting renal tubular acidosis [hp:0004910]
Bicarbonate-wasting renal tubular acidosis

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.

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.
Dense posterior cortical cataract [hp:0007948]

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.

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.
Abnormality of the vertebrae [hp:0003468]

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.
Metacarpophalangeal joint contracture [hp:0006070]

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.
Loss of ability to walk in first decade [hp:0006794]

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.
2nd-5th toe middle phalangeal hypoplasia [hp:0008083]
2nd-5th toe middle phalangeal hypoplasia

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.

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.

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.

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.
Increased urinary cortisol level [hp:0012030]

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.
Desquamative interstitial pneumonitis [hp:0005942]

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.

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.
Gastrointestinal telangiectasia [hp:0002604]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Increased intramuscular fat [hp:0008985]

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.

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.

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.

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.
Broad secondary alveolar ridge [hp:0000216]

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.

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.

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.
Long-chain dicarboxylic aciduria [hp:0008293]

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.
Impaired distal tactile sensation [hp:0006937]

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.

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.

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.

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.
Polyostotic fibrous dysplasia [hp:0010735]

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.
Radial deviation of thumb terminal phalanx [hp:0005895]
Radial deviation of thumb terminal phalanx

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.

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.

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.

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.
Amyotrophy of ankle musculature [hp:0009031]

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.
Abnormal form of the vertebral bodies [hp:0003312]

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.

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.

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.

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.

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.
Short stepped shuffling gait [hp:0007311]

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.
Loss of facial adipose tissue [hp:0000292]

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.
Progressive spastic quadriplegia [hp:0002478]

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.
Increased laxity of fingers [hp:0006149]

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.

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.

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.

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.
Abnormality of circulating hormone level [hp:0003117]
Abnormality of circulating hormone level

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.

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.
Obliteration of the pulp chamber [hp:0006350]

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.

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.
Abnormality of mitochondrial metabolism [hp:0003287]

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.

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.

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.
Pigment deposition in the trabecular meshwork [hp:0012631]
Pigment deposition in the trabecular meshwork

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.
Neuronal loss in the cerebral cortex [hp:0007190]

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.

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.
Abnormality of the gastric mucosa [hp:0004295]

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.
Opacification of the corneal epithelium [hp:0007727]

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.

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.

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.

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.

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.

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.

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.
Neoplasm of the adrenal cortex [hp:0100641]

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.
Intimal thickening in the coronary arteries [hp:0005292]
Intimal thickening in the coronary arteries

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.
Impaired collagen-induced platelet aggregation [hp:0008320]
Impaired collagen-induced platelet aggregation

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.

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.

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.

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.
Severe generalized osteoporosis [hp:0005897]

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.

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.

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.
Hypoplasia of the tooth germ [hp:0006353]

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.
Abnormality of the odontoid process [hp:0003310]

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.
Decreased sensitivity to hypoxemia [hp:0005947]

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.

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.

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.
Increased circulating cortisol level [hp:0003118]

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.

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.

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.
Conductive hearing impairment [hp:0000405]

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.

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.

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.

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.
Abnormality of the fingernails [hp:0001231]

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.

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.

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.

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.
Aplasia/Hypoplasia of the nipples [hp:0006709]

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.

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.
Impaired vibration sensation at ankles [hp:0006938]

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.
Abnormality of the forehead [hp:0000290]

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.
Primitive reflexes (palmomental, snout, glabellar) [hp:0002476]
Primitive reflexes (palmomental, snout, glabellar)

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.

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.
Multicentric ossification of proximal femoral epiphyses [hp:0006450]
Multicentric ossification of proximal femoral epiphyses

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.
Ventilator dependence with inability to wean [hp:0005946]
Ventilator dependence with inability to wean

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.
Failure of eruption of permanent teeth [hp:0006352]

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.
Abnormality of lipid metabolism [hp:0003119]

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.
Widely patent coronal suture [hp:0005442]

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.
Hypoplasia of the odontoid process [hp:0003311]

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.

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.

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.

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.
Neoplasm of the central nervous system [hp:0100006]

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.
Triangular shaped proximal phalanx of the 3rd finger [hp:0009456]
Triangular shaped proximal phalanx of the 3rd finger

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.
Abnormality of the peritoneum [hp:0002585]

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.

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.
Abnormal mitochondrial morphology [hp:0008322]

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.
Yellow subcutaneous tissue covered by thin, scaly skin [hp:0007525]
Yellow subcutaneous tissue covered by thin, scaly skin

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.

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.

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.

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.
Axillary apocrine gland hypoplasia [hp:0007397]

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.

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.

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.

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.

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.

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.
White matter neuronal heterotopia [hp:0007314]

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.
Premature peripheral vascular disease [hp:0005299]

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.
Metacarpophalangeal synostosis [hp:0005880]

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.
Ventricular preexcitation with multiple accessory pathways [hp:0006684]
Ventricular preexcitation with multiple accessory pathways

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.

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.
Abnormality of the enteric ganglia [hp:0004362]

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.

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.

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.
Generalized tonic-clonic seizures on awakening [hp:0007193]
Generalized tonic-clonic seizures on awakening

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.

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.

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.

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.
Abnormal rod and cone electroretinograms [hp:0008323]
Abnormal rod and cone electroretinograms

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.
Multicentric femoral head ossification [hp:0008835]

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.

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.

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.

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.

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.

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.

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.
Prominent supraorbital ridges [hp:0000336]

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.

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.
Abnormality of the left ventricle [hp:0001711]

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.

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.
Recurrent mandibular subluxations [hp:0005332]

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.

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.

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.
Adenomatous colonic polyposis [hp:0005227]

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.

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.
Hyporeflexia of upper limbs [hp:0012391]

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.
Aplasia/Hypoplasia of the phalanges of the toes [hp:0010173]
Aplasia/Hypoplasia of the phalanges of the toes

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.

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.

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.

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.

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.

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.
Involuntary writhing movements [hp:0007316]

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.
Stippled calcification proximal humeral epiphyses [hp:0008838]
Stippled calcification proximal humeral epiphyses

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.

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.
Left ventricular hypertrophy [hp:0001712]

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.

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.

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.

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.

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.

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.
Prominent superficial blood vessels [hp:0007394]

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.

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.

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.

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.

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.

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.

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.
Abnormality of the pulmonary artery [hp:0004414]

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.

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.

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.
Hypopigmented skin patches on arms [hp:0007526]

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.

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.

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.

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.

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.
Stenosis of the external auditory canal [hp:0000402]

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.
Absent atrioventricular node [hp:0006681]

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.

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.

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.
Atrioventricular canal defect with right ventricle aorta and pulmonary atresia [hp:0005298]
Atrioventricular canal defect with right ventricle aorta and pulmonary atresia

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.

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.

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.

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.
Profound sensorineural hearing impairment [hp:0011476]
Profound sensorineural hearing impairment

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.

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.

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.

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.

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.
Dilatation of the ascending aorta [hp:0005111]

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.
Elevated urine pyrophosphate [hp:0003491]

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.
Nonprogressive restrictive external ophthalmoplegia [hp:0007831]
Nonprogressive restrictive external ophthalmoplegia

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.

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.

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.

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.
Urinary glycosaminoglycan excretion [hp:0003541]

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.

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.
Premature coronary artery disease [hp:0005181]

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.

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.
Aplasia/Hypoplasia of the middle phalanges of the toes [hp:0010194]
Aplasia/Hypoplasia of the middle phalanges of the toes

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.

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.

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.

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.

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.

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.

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.

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.
Abnormality of the epididymis [hp:0009714]

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.
Loss of gluteal subcutaneous adipose tissue [hp:0009017]
Loss of gluteal subcutaneous adipose tissue

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.
Agenesis of permanent teeth [hp:0006349]

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.
Abnormality of peripheral nerve conduction [hp:0003134]
Abnormality of peripheral nerve conduction

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.

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.

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.

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.

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.

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.

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.
High urinary gonadotropins (primary hypogonadism) [hp:0003492]
High urinary gonadotropins (primary hypogonadism)

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.
Impaired platelet aggregation [hp:0003540]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Papillary cystadenoma of the epididymis [hp:0009715]

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.

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.
Abnormality of the spinocerebellar tracts [hp:0003133]
Abnormality of the spinocerebellar tracts

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.

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.

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.

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.
Decreased mean platelet volume [hp:0005537]

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.
Screwdriver-shaped incisors [hp:0006346]

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.

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.
Enlarged vertebral pedicles [hp:0004621]

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.
Fused fourth and fifth metacarpals [hp:0005867]

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.

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.
Antinuclear antibody positivity [hp:0003493]

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.
Abnormality of mucopolysaccharide metabolism [hp:0011020]
Abnormality of mucopolysaccharide metabolism

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.

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.

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.

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.
Abnormality of zinc homeostasis [hp:0008277]

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.
Thoracolumbar interpediculate narrowness [hp:0008484]
Thoracolumbar interpediculate narrowness

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.

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.

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.

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.

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.
Decreased serum complement C9 [hp:0012308]

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.
Right ventricular hypertrophy [hp:0001667]

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.

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.
Amegakaryocytic thrombocytopenia [hp:0004859]

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.

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.

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.

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.

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.
Nonprogressive cerebellar ataxia [hp:0002470]

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.

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.
Microdontia of primary teeth [hp:0006347]

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.

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.
Lambdoidal craniosynostosis [hp:0004443]

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.

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.

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.
Metaphyseal enchondromatosis [hp:0005868]

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.
Segmental peripheral demyelination/remyelination [hp:0003481]
Segmental peripheral demyelination/remyelination

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.
Asymmetry of spinal facet joints [hp:0008482]

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.

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.
Cerebellar cortical atrophy [hp:0008278]

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.

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.
Second metatarsal posteriorly placed [hp:0008125]

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.

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.
Upper limb muscle hypoplasia [hp:0009016]

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.

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.

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.

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.

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.

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.

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.
Proximal symphalangism (hands) [hp:0006152]

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.
Dysplastic distal thumb phalanges with a central hole [hp:0005688]
Dysplastic distal thumb phalanges with a central hole

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.

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.
Underdeveloped superior crus of antihelix [hp:0011246]
Underdeveloped superior crus of antihelix

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.

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.
Increased sensitivity to ionizing radiation [hp:0011133]
Increased sensitivity to ionizing radiation

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.
Abnormality of primary molar morphology [hp:0006344]

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.
Hyperchromic macrocytic anemia [hp:0004857]

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.

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.
Supraventricular arrhythmia [hp:0005115]

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.
Downturned corners of mouth [hp:0002714]

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.

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.
Chin with horizontal crease [hp:0011823]

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.

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.

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.

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.

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.
Autosomal dominant contiguous gene syndrome [hp:0001452]
Autosomal dominant contiguous gene syndrome

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.

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.

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.

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.

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.
Spinocerebellar tract degeneration [hp:0002503]

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.
Abnormal cone-mediated electroretinogram [hp:0008275]
Abnormal cone-mediated electroretinogram

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.

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.

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.
Periosteal thickening of long tubular bones [hp:0006465]
Periosteal thickening of long tubular bones

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.
Opposable triphalangeal thumb [hp:0005866]

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.

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.
Increased blood urea nitrogen (BUN) [hp:0003138]

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.
Hump-shaped mound of bone in central and posterior portions of vertebral endplate [hp:0004594]
Hump-shaped mound of bone in central and posterior portions of vertebral endplate

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.

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.
Hypoplasia of the corpus callosum [hp:0002079]

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.

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.
Multiple joint contractures [hp:0002828]

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.

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.
Abnormality of the immune system [hp:0002715]

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.

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.

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.

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.

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.

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.
Early onset of sexual maturation [hp:0100000]

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.
Finger joint hyperextensibility [hp:0006158]

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.

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.

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.
Onycholysis of distal fingernails [hp:0008400]

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.

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.

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.
Peg-shaped maxillary lateral incisors [hp:0006342]

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.

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.
Dilatation of the aortic arch [hp:0005113]

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.

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.
Shoulder girdle muscle weakness [hp:0003547]

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.

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.

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.
Increased serum beta-hexosaminidase [hp:0003333]

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.
Abnormality of the gastrointestinal tract [hp:0011024]
Abnormality of the gastrointestinal tract

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.

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.

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.

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.

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.
Neoplasm of the endocrine system [hp:0100568]

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.
Cerebral amyloid angiopathy [hp:0011970]

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.

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.

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.

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.

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.

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.

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.
Antegonial notching of mandible [hp:0003779]

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.

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.
Spasticity of pharyngeal muscles [hp:0002501]

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.

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.
Adult-onset night blindness [hp:0007830]

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.

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.

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.

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.

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.

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.

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.
Defective dehydrogenation of isovaleryl CoA and butyryl CoA [hp:0003490]
Defective dehydrogenation of isovaleryl CoA and butyryl CoA

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.
Absent primary metaphyseal spongiosa [hp:0003332]

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.
Abnormality of cardiovascular system physiology [hp:0011025]
Abnormality of cardiovascular system physiology

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.

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.

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.

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.
Loss of retinal pigment epithelium [hp:0007722]

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.

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.
Hypoplasia of serratus anterior muscle [hp:0009011]

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.

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.
Normochromic microcytic anemia [hp:0004856]

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.
Abnormal vertebral ossification [hp:0100569]

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.

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.
Abnormality of the umbilicus [hp:0001551]

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.

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.

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.

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.
Abnormality of the cerebral white matter [hp:0002500]
Abnormality of the cerebral white matter

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.

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.

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.
Antenatal intracerebral hemorrhage [hp:0007023]

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.

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.
Congenital hepatic fibrosis [hp:0002612]

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.

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.

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.

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.

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.

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.
Orthostatic hypotension due to autonomic dysfunction [hp:0004926]
Orthostatic hypotension due to autonomic dysfunction

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.
Ivory epiphyses of the distal phalanges of the hand [hp:0010252]
Ivory epiphyses of the distal phalanges of the hand

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.

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.

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.
Abnormality of brainstem morphology [hp:0002363]

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.

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.
Recurrent bacterial infections [hp:0002718]

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.

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.
Abnormality of connective tissue [hp:0003549]

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.

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.

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.

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.

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.
Intrahepatic cholestasis with episodic jaundice [hp:0006575]
Intrahepatic cholestasis with episodic jaundice

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.
Absent or minimally ossified vertebral bodies [hp:0004599]
Absent or minimally ossified vertebral bodies

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.

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.

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.

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.

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.
Abnormal foot bone ossification [hp:0010675]

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.

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.

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.

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.

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.

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.
Pulmonary artery dilatation [hp:0004927]

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.
Aplasia/Hypoplasia involving the nose [hp:0009924]

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.
Thyroid hormone receptor defect [hp:0002930]

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.

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.

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.

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.

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.

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.

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.
Subsarcolemmal accumulations of abnormally shaped mitochondria [hp:0003548]
Subsarcolemmal accumulations of abnormally shaped mitochondria

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.

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.
Intermittent thrombocytopenia [hp:0004854]

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.
Femoral bowing present at birth, straightening with time [hp:0005005]
Femoral bowing present at birth, straightening with time

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.

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.
Hepatic arteriovenous malformation [hp:0006574]

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.

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.

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.

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.
Supernumerary vertebral ossification centers [hp:0004598]
Supernumerary vertebral ossification centers

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.
Progressive spastic paraplegia [hp:0007020]

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.
Small cervical vertebral bodies [hp:0004629]

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.
Broad distal phalanx of the thumb [hp:0009642]

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.
Hypoplasia of the brainstem [hp:0002365]

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.

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.
Abnormality of the urinary system [hp:0000079]

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.

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.
Abnormality of thrombocytes [hp:0001872]

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.

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.
Abnormal oral glucose tolerance [hp:0004924]

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.
Elevated diastolic blood pressure [hp:0005117]

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.
Folate-responsive megaloblastic anemia [hp:0004851]

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.

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.

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.
Sternocleidomastoid amyotrophy [hp:0012036]

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.

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.

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.

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.

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.

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.
Decreased muscle glycogen content [hp:0012270]

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.

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.

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.

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.
Stage 5 chronic kidney disease [hp:0003774]

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.

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.

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.

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.
Abnormality of blood and blood-forming tissues [hp:0001871]
Abnormality of blood and blood-forming tissues

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.

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.

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.
Abnormal upper motor neuron morphology [hp:0002127]

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.

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.

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.
Spinous keratoses of palms and soles [hp:0007613]

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.

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.
Acute episodes of neuropathic symptoms [hp:0003489]

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.

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.

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.

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.
Osteolysis involving tarsal bones [hp:0006234]

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.

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.
Subacute progressive viral hepatitis [hp:0006572]

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.
Aplasia of the sweat glands [hp:0011136]

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.
Episodic upper airway obstruction [hp:0012271]

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.
Aplasia/Hypoplasia of the capital femoral epiphysis [hp:0005003]
Aplasia/Hypoplasia of the capital femoral epiphysis

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.

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.

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.
Increased circulating gonadotropin level [hp:0000837]
Increased circulating gonadotropin level

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.

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.
Acroosteolysis of distal phalanges (feet) [hp:0001870]
Acroosteolysis of distal phalanges (feet)

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.

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.

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.

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.

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.

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.
Hyperextensibility at wrists [hp:0005072]

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.
Facial capillary hemangioma [hp:0000996]

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.

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.

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.

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.

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.

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.

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.
Hamartomatous stomach polyps [hp:0004795]

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.

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.

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.
GM2-ganglioside accumulation [hp:0003495]

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.

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.

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.

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.
Swan neck-like deformities of the fingers [hp:0006150]
Swan neck-like deformities of the fingers

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.

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.
Prolonged neonatal jaundice [hp:0006579]

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.

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.

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.
Aminoglycoside-induced hearing loss [hp:0011975]

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.

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.

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.
Prenatal movement abnormality [hp:0001557]

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.
Distal/middle symphalangism of 5th finger [hp:0009244]
Distal/middle symphalangism of 5th finger

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.
Insulin-resistant diabetes mellitus [hp:0000831]

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.

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.

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.

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.

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.

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.

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.
Abnormality of extrapyramidal motor function [hp:0002071]
Abnormality of extrapyramidal motor function

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.
Recurrent deep vein thrombosis [hp:0004850]

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.
Limited extraocular movements [hp:0007941]

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.
Recurrent systemic pyogenic infections [hp:0005429]

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.

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.
Increased carotid artery intimal medial thickness [hp:0012273]
Increased carotid artery intimal medial thickness

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.
Unilateral vestibular Schwannoma [hp:0009590]

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.

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.

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.

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.
Abnormal peripheral myelination [hp:0003130]

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.

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.

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.

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.

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.
Hypopigmentation of the skin [hp:0001010]

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.

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.

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.

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.
Progressive loss of facial adipose tissue [hp:0009019]
Progressive loss of facial adipose tissue

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.
Progressive reticulate hyperpigmentation [hp:0007456]
Progressive reticulate hyperpigmentation

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.
Peripheral arterial stenosis [hp:0004928]

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.

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.

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.
Anterior rounding of vertebral bodies [hp:0008488]

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.
Pericardial lymphangiectasia [hp:0005183]

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.

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.

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.
Abnormality of the adrenal glands [hp:0000834]

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.

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.

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.

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.

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.

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.
Increased neuronal autofluorescent lipopigment [hp:0002074]
Increased neuronal autofluorescent lipopigment

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.
Blotching pigmentation of the skin [hp:0007610]

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.

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.
Elevated urinary vanillylmandelic acid [hp:0011978]

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.
Prominent interphalangeal joints [hp:0006237]

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.

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.

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.

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.
Cone-shaped epiphyses of the middle phalanges of the hand [hp:0010259]
Cone-shaped epiphyses of the middle phalanges of the hand

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.
Aldehyde oxidase deficiency [hp:0002932]

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.

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.

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.

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.
Hyperplasia of the femoral trochanters [hp:0002822]

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.

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.
Morphological abnormality of the middle ear [hp:0008609]
Morphological abnormality of the middle ear

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.

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.

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.
Enhancement of the C-reflex [hp:0001340]

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.

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.
Autosomal dominant inheritance with maternal imprinting [hp:0012275]
Autosomal dominant inheritance with maternal imprinting

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.

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.

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.

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.
Calf muscle pseudohypertrophy [hp:0003707]

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.
Hepatic vascular malformations [hp:0006576]

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.
Progressive cerebellar ataxia [hp:0002073]

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.
Elevated urinary homovanillic acid [hp:0011977]

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.

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.
Gastrointestinal obstruction [hp:0004796]

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.
Disproportionate short stature [hp:0003498]

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.

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.
Aplasia of the tarsal bones [hp:0010509]

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.
Congenital stapes ankylosis [hp:0007943]

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.

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.

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.
Aplasia/Hypoplasia of the thymus [hp:0010515]

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.
Madelung-like forearm deformities [hp:0003068]

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.

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.
Regional abnormality of skin [hp:0011356]

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.

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.

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.
Recurrent infections in infancy and early childhood [hp:0005437]
Recurrent infections in infancy and early childhood

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.
Diffuse spongiform leukoencephalopathy [hp:0006943]

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.

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.

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.

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.

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.

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.
Bilateral sensorineural hearing impairment [hp:0008619]
Bilateral sensorineural hearing impairment

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.

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.

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.
Abnormality of the diaphragm [hp:0000775]

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.

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.

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.

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.

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.

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.
Premature separation of centromeric heterochromatin [hp:0003616]
Premature separation of centromeric heterochromatin

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.
1-5 finger complete cutaneous syndactyly [hp:0006088]
1-5 finger complete cutaneous syndactyly

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.

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.

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.
Short middle phalanx of the 5th finger [hp:0004220]

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.

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.
Hypoplastic olfactory lobes [hp:0006894]

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.
Bilateral congenital mydriasis [hp:0007932]

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.

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.

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.

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.

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.

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.

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.

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.
Abnormality of parotid gland [hp:0000197]

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.

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.

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.
Abnormality of branched chain family amino acid metabolism [hp:0010892]
Abnormality of branched chain family amino acid metabolism

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.

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.

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.
Hypoplasia of the fallopian tube [hp:0008697]

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.

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.
Abnormality of skin pigmentation [hp:0001000]

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.

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.

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.

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.

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.

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.
Increased prevalence of valvular disease [hp:0001726]
Increased prevalence of valvular disease

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.
Juvenile posterior subcapsular lenticular opacities [hp:0007935]
Juvenile posterior subcapsular lenticular opacities

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.
Congenital thrombocytopenia [hp:0001905]

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.
Hurthle cell thyroid adenoma [hp:0006781]

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.

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.

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.

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.
Extension of hair growth on temples to lateral eyebrow [hp:0005325]
Extension of hair growth on temples to lateral eyebrow

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.

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.

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.

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.
Acral ulceration and osteomyelitis leading to autoamputation of digits [hp:0001226]
Acral ulceration and osteomyelitis leading to autoamputation of digits

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.

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.

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.
Ulnar deviation of the 2nd finger [hp:0009464]

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.

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.
Repetitive compulsive behavior [hp:0008762]

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.

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.

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.

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.

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.
Progressive central visual loss [hp:0008008]

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.

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.

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.
Frontotemporal cerebral atrophy [hp:0006892]

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.

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.

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.

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.

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.
Antiphospholipid antibody positivity [hp:0003613]

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.
Abnormality of alkaline phosphatase activity [hp:0004379]
Abnormality of alkaline phosphatase activity

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.
Radial deviation of the 3rd finger [hp:0009462]

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.

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.

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.

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.
Disturbance of facial expression [hp:0005324]

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.

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.
Primary congenital glaucoma [hp:0008007]

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.

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.

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.

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.
Congenital diaphragmatic hernia [hp:0000776]

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.
Rapid neurologic deterioration [hp:0007307]

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.

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.

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.

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.

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.
Ulnar deviation of the 3rd finger [hp:0009463]

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.

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.

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.

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.

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.
Midface capillary hemangioma [hp:0007452]

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.
Abnormality of the heme biosynthetic pathway [hp:0010472]
Abnormality of the heme biosynthetic pathway

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.

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.

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.

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.

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.

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.
Expanded metacarpals with widened medullary cavities [hp:0006232]
Expanded metacarpals with widened medullary cavities

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.

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.

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.
Positive ferric chloride test [hp:0003612]

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.

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.
Honeycomb retinal degeneration [hp:0007937]

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.

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.
Hypohidrotic ectodermal dysplasia [hp:0007607]

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.

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.
Abnormality of erythrocytes [hp:0001877]

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.

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.

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.

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.
Triangular shaped proximal phalanx of the 2nd finger [hp:0009587]
Triangular shaped proximal phalanx of the 2nd finger

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.

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.

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.

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.

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.
Adult onset sensorineural hearing impairment [hp:0008615]
Adult onset sensorineural hearing impairment

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.
Inappropriate sexual behavior [hp:0008768]

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.

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.
Lethal short-limbed short stature [hp:0008909]

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.

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.

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.

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.
Reduced number of intrahepatic bile ducts [hp:0006571]
Reduced number of intrahepatic bile ducts

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.
Everted upper lip vermilion [hp:0010803]

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.
Abnormality of epiphysis morphology [hp:0005930]

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.

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.

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.

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.

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.

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.
Abnormality of the parathyroid gland [hp:0000828]

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.

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.
Malignant eosinophil proliferation [hp:0006782]

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.
Restrictive external ophthalmoplegia [hp:0007936]

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.

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.

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.

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.
Punctate palmoplantar hyperkeratosis [hp:0007530]

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.
Abnormality of the eyelashes [hp:0000499]

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.
Persistent pupillary membrane [hp:0009917]

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.

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.

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.
Abnormality of the frontal sinuses [hp:0002687]

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.

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.

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.

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.

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.
Epilepsia partialis continua [hp:0012847]

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.
Congenital corneal dystrophy [hp:0008005]

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.
Hypotrophy of the small hand muscles [hp:0006006]

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.

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.

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.
Medially deviated second toe [hp:0008096]

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.

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.

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.

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.

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.

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.

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.
Limb-girdle muscular dystrophy [hp:0006785]

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.
Basal ganglia calcification [hp:0002135]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Abnormality of the sense of smell [hp:0004408]

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.

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.

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.

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.
Prenatal maternal abnormality [hp:0002686]

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.

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.

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.
Progeroid facial appearance [hp:0005328]

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.

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.

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.
Abnormality of the basal ganglia [hp:0002134]

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.

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.

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.

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.

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.

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.

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.
Self-mutilation of tongue and lips due to involuntary movements [hp:0008767]
Self-mutilation of tongue and lips due to involuntary movements

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.

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.
Hepatic periportal necrosis [hp:0002614]

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.
Jerky ocular pursuit movements [hp:0008003]

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.

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.

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.

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.
Late-onset distal muscle weakness [hp:0003810]

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.
Abnormality of macular pigmentation [hp:0008002]

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.
Severe intrauterine growth retardation [hp:0008846]

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.

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.
Gastrointestinal dysmotility [hp:0002579]

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.

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.

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.
Interphalangeal joint contracture of finger [hp:0001220]
Interphalangeal joint contracture of finger

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.

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.
Abnormality of eye movement [hp:0000496]

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.
Increased urinary hypoxanthine [hp:0011814]

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.
Prolonged whole-blood clotting time [hp:0005542]

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.
Ankylosis of feet small joints [hp:0008090]

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.

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.

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.
Reduced consciousness/confusion [hp:0004372]

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.

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.
Spontaneous, recurrent epistaxis [hp:0004406]

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.
U-Shaped upper lip vermilion [hp:0010806]

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.
Proximal femoral epiphysiolysis [hp:0006461]

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.

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.

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.
Short distal phalanx of the 5th finger [hp:0004227]

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.

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.
Accumulation of melanosomes in melanocytes [hp:0001008]
Accumulation of melanosomes in melanocytes

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Neoplasia of the nasopharynx [hp:0100630]

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.
Clusters of axonal regeneration [hp:0007233]

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.

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.
Exercise-induced muscle fatigue [hp:0009020]

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.
Decreased/absent ankle reflexes [hp:0200101]

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.
Recurrent Neisserial infections [hp:0005430]

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.

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.

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.
Progressive muscle weakness [hp:0003323]

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.

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.
Short proximal phalanx of hallux [hp:0010107]

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.

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.

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.

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.

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.

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.
Duplication of internal organs [hp:0005217]

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.

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.
Semilobar holoprosencephaly [hp:0002507]

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.
Generalized bone demineralization [hp:0006462]

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.

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.

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.
Unconjugated hyperbilirubinemia [hp:0008282]

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.

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.
Bilateral vestibular Schwannoma [hp:0009589]

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.
Episodic peripheral neuropathy [hp:0006949]

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.
Abnormality of oral frenula [hp:0000190]

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.
Calcification of the small brain vessels [hp:0002504]
Calcification of the small brain vessels

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.
Reduced von Willebrand factor activity [hp:0008330]

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.

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.

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.
Proximal muscle weakness in upper limbs [hp:0008997]

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.

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.
Ectopic posterior pituitary [hp:0011755]

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.
Recurrent subcortical infarcts [hp:0007236]

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.

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.

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.
Abnormality of temperature regulation [hp:0004370]

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.
Generalized muscle weakness [hp:0003324]

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.

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.

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.

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.
Fusion of the cerebellar hemispheres [hp:0006899]

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.

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.

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.

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.

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.

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.

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.
Mitochondrial encephalopathy [hp:0006789]

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.

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.
Medial flaring of the eyebrow [hp:0010747]

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.

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.

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.

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.

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.

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.
Diffuse retinal cone degeneration [hp:0007829]

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.
Infantile sensorineural hearing impairment [hp:0008610]
Infantile sensorineural hearing impairment

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.

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.

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.

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.
Metaphyseal chondrodysplasia [hp:0005871]

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.
Limb-girdle muscle weakness [hp:0003325]

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.

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.

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.
Absence of intrinsic factor [hp:0005219]

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.

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.

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.
Progressive inability to walk [hp:0002505]

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.

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.

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.

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.
Atresia of the external auditory canal [hp:0000413]

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.
Decreased distal sensory nerve action potential [hp:0007230]
Decreased distal sensory nerve action potential

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.
Reduced erythrocyte 2,3-diphosphoglycerate concentration [hp:0030271]
Reduced erythrocyte 2,3-diphosphoglycerate concentration

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.

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.
Aplasia/Hypoplasia of the distal phalanges of the toes [hp:0010185]
Aplasia/Hypoplasia of the distal phalanges of the toes

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Increased red cell osmotic resistance [hp:0005546]

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.

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.
Impaired myocardial contractility [hp:0006670]

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.
Type II transferrin isoform profile [hp:0012301]

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.

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.

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.

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.

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.

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.

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.
Elevated red cell adenosine deaminase activity [hp:0030270]
Elevated red cell adenosine deaminase activity

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.
Proximal muscle weakness in lower limbs [hp:0008994]

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.
Duplicated collecting system [hp:0000081]

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.
Triangular epiphysis of the proximal phalanx of the 3rd finger [hp:0009356]
Triangular epiphysis of the proximal phalanx of the 3rd finger

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.
Abnormal respiratory motile cilium morphology [hp:0005938]
Abnormal respiratory motile cilium morphology

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.

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.
Pointed proximal second through fifth metacarpals [hp:0001223]
Pointed proximal second through fifth metacarpals

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.

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.

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.

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.
Depletion of mitochondrial DNA in muscle tissue [hp:0009141]
Depletion of mitochondrial DNA in muscle tissue

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.
Submucous cleft soft palate [hp:0011819]

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.

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.
Myeloproliferative disorder [hp:0005547]

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.
Hyperostosis frontalis interna [hp:0004438]

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.

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.

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.

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.
Herpes simplex encephalitis [hp:0012302]

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.

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.
Transposition of the great arteries [hp:0001669]

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.

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.
Spinocerebellar tract disease in lower limbs [hp:0007232]
Spinocerebellar tract disease in lower limbs

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.
Aplasia cutis congenita of scalp [hp:0007385]

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.
Increased serum free triiodothyronine (fT3) [hp:0011788]
Increased serum free triiodothyronine (fT3)

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.

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.

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.
Neoplasm of the adrenal gland [hp:0100631]

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.
Increased intraabdominal fat [hp:0008993]

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.

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.
High-output congestive heart failure [hp:0001722]

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.

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.

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.

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.

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.
Reduced red cell adenosine deaminase activity [hp:0030273]
Reduced red cell adenosine deaminase activity

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.
Downslanted palpebral fissures [hp:0000494]

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.

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.
Abnormality of reproductive system physiology [hp:0000080]
Abnormality of reproductive system physiology

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.

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.
Abnormality of the hip bone [hp:0003272]

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.
Predominantly lower limb lymphedema [hp:0003550]

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.

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.
Congenital posterior urethral valve [hp:0010957]

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.

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.

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.

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.

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.

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.

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.

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.
Aberrant melanosome maturation [hp:0007384]

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.

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.

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.

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.
Radial deviation of the 2nd finger [hp:0009467]

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.

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.

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.

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.

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.
Multinucleated giant chondrocytes in epiphyseal cartilage [hp:0030330]
Multinucleated giant chondrocytes in epiphyseal cartilage

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.

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.

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.

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.

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.

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.
Frequent Giardia lamblia infestation [hp:0005215]

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.

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.
Retinal vascular tortuosity [hp:0012841]

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.
Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes [hp:0003329]
Hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes

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.
Paroxysmal atrial tachycardia [hp:0006671]

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.
Congenital localized absence of skin [hp:0007383]

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.

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.
Neoplasm of the nervous system [hp:0004375]

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.

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.
Hypoplasia of olfactory tract [hp:0007036]

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.

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.

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.
Thick anterior alveolar ridges [hp:0009100]

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.
Nephrogenic diabetes insipidus [hp:0009806]

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.

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.

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.

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.
Acral ulceration leading to autoamputation of digits [hp:0006121]
Acral ulceration leading to autoamputation of digits

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.

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.
Leydig cell insensitivity to gonadotropin [hp:0002929]
Leydig cell insensitivity to gonadotropin

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.

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.
Elevated urinary norepinephrine [hp:0003345]

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.

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.

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.
Abnormality of the middle ear ossicles [hp:0004452]

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.
Opacification of the corneal stroma [hp:0007759]

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.

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.

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.

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.

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.
Proximal fibular overgrowth [hp:0005067]

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.

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.

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.

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.
Impaired visuospatial constructive cognition [hp:0010794]
Impaired visuospatial constructive cognition

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.

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.

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.

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.
Giant somatosensory evoked potentials [hp:0001312]

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.
Abnormal iron deposition in mitochondria [hp:0008306]
Abnormal iron deposition in mitochondria

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.

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.
Nasolacrimal duct obstruction [hp:0000579]

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.

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.
Congenital visual impairment [hp:0007758]

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.

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.

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.

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.

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.
Viral infection-induced rhabdomyolysis [hp:0003558]

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.
Decreased activity of the pyruvate dehydrogenase (PDH) complex [hp:0002928]
Decreased activity of the pyruvate dehydrogenase (PDH) complex

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.

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.
Displacement of the external urethral meatus [hp:0100627]
Displacement of the external urethral meatus

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.

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.

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.

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.

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.
Proximal tibial hypopolasia [hp:0006379]

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.
Absent styloid process of ulna [hp:0005068]

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.
Pseudoepiphyses of the metacarpals [hp:0009193]

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.

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.
Anterior open-bite malocclusion [hp:0009102]

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.

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.

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.

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.

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.

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.
Abnormality of the pericardium [hp:0001697]

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.

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.
Medium chain dicarboxylic aciduria [hp:0008309]

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.
Abnormal nervous system electrophysiology [hp:0001311]
Abnormal nervous system electrophysiology

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.

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.

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.

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.
Abnormal middle ear reflexes [hp:0004454]

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.

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.

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.
Increased variability in muscle fiber diameter [hp:0003557]
Increased variability in muscle fiber diameter

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.
Hypersegmentation of neutrophil nuclei [hp:0004821]

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.

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.
Glutathione synthetase deficiency [hp:0003343]

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.

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.

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.
Abnormal cortical bone morphology [hp:0003103]

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.

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.
Neutrophil inclusion bodies [hp:0008264]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Overfolding of the superior helices [hp:0004453]

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.
Abnormality of the duodenum [hp:0002246]

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.

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.

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.
Thyroid defect in oxidation and organification of iodide [hp:0008263]
Thyroid defect in oxidation and organification of iodide

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.

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.

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.

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.
Abnormal immunoglobulin level [hp:0010701]

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.

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.
Corpus cavernosum sclerosis [hp:0100624]

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.

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.

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.
Aplasia of the phalanges of the hand [hp:0009802]

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.

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.

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.

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.

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.

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.
Fragmented, irregular epiphyses [hp:0005063]

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.
Posterior scalloping of vertebral bodies [hp:0005121]
Posterior scalloping of vertebral bodies

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.
Multiple prenatal fractures [hp:0005855]

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.
Trapezoidal distal femoral condyles [hp:0006432]

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.

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.

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.
Juvenile epithelial corneal dystrophy [hp:0007755]

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.

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.
Abnormality of the cerebellum [hp:0001317]

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.

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.

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.
Thyroid-stimulating hormone excess [hp:0002925]

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.

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.
Symmetric lesions of the basal ganglia [hp:0007039]

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.
Hyperactive renin-angiotensin system [hp:0000841]

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.
Delayed eruption of primary teeth [hp:0000680]

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.
Reduced thyroxin-binding globulin [hp:0012509]

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.

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.
Edema of the dorsum of feet [hp:0012098]

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.
Single transverse palmar crease [hp:0000954]

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.
Proximal femoral metaphyseal abnormality [hp:0006431]
Proximal femoral metaphyseal abnormality

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.

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.

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.

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.

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.
Decreased circulating aldosterone level [hp:0002924]

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.
Type 2 muscle fiber atrophy [hp:0003554]

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.

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.

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.

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.
Episodic ammonia intoxication [hp:0001951]

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.

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.
Neoplasm of the thyroid gland [hp:0100031]

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.
Exercise-induced myoglobinuria [hp:0008305]

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.

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.

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.

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.

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.

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.
Hyperpigmentation of the skin [hp:0000953]

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.

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.
Anterior clefting of vertebral bodies [hp:0009761]

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.

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.
Hypoplasia of proximal radius [hp:0006434]

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.

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.

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.
Anterior concavity of thoracic vertebrae [hp:0004611]
Anterior concavity of thoracic vertebrae

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.
Dilatated internal auditory canal [hp:0004458]

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.
Cellulitis due to immunodeficiency [hp:0003553]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Folate-unresponsive megaloblastic anemia [hp:0004826]
Folate-unresponsive megaloblastic anemia

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Follicular thyroid carcinoma [hp:0006731]

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.
Decreased serum complement factor B [hp:0005416]

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.

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.

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.

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.

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.

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.
Hemihypotrophy of lower limb [hp:0200053]

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.
Muscular subvalvular aortic stenosis [hp:0001691]

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.

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.
Distal upper limb amyotrophy [hp:0007149]

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.
Short distal phalanx of the thumb [hp:0009650]

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.
Abnormality of saccadic eye movements [hp:0000570]

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.
Increased red cell hemolysis by shear stress [hp:0008269]
Increased red cell hemolysis by shear stress

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.

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.

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.

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.

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.

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.

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.
Abnormality of the temporal bone [hp:0009911]

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.

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.

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.
Gaze-evoked horizontal nystagmus [hp:0007979]

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.
Increased serum bile acid concentration [hp:0012202]

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.

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.

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.

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.

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.
Abnormal vestibulo-ocular reflex [hp:0007670]

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.

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.
Decreased number of CD8+ T cells [hp:0005415]

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.

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.

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.

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.

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.

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.
Decreased circulating ACTH level [hp:0002920]

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.

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.

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.
Abnormality of the rib cage [hp:0001547]

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.
Congenital sensorineural hearing impairment [hp:0008527]
Congenital sensorineural hearing impairment

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.

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.

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.
Denervation of the diaphragm [hp:0009109]

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.

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.

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.

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.

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.
Recurrent mycobacterial infections [hp:0011274]

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.
Reduced prothrombin activity [hp:0012201]

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.

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.
Enlargement of the distal femoral epiphysis [hp:0006438]
Enlargement of the distal femoral epiphysis

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.
Acute megakaryocytic leukemia [hp:0006733]

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.
Hyperapobetalipoproteinemia [hp:0008158]

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.
Limited elbow flexion/extension [hp:0005060]

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.

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.

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.

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.

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.
Intervertebral disc degeneration [hp:0008419]

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.

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.

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.

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.

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.

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.

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.
Disproportionate prominence of the femoral medial condyle [hp:0006437]
Disproportionate prominence of the femoral medial condyle

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.

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.

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.

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.
Weakness of facial musculature [hp:0030319]

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.
Recurrent mycobacterium avium complex infections [hp:0011275]
Recurrent mycobacterium avium complex infections

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.

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.

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.

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.
Triangular epiphysis of the proximal phalanx of the 2nd finger [hp:0009534]
Triangular epiphysis of the proximal phalanx of the 2nd finger

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.
Percussion-induced rapid rolling muscle contractions (PIRC) [hp:0003760]
Percussion-induced rapid rolling muscle contractions (PIRC)

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.

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.

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.

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.

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.
Axial malrotation of the kidney [hp:0004717]

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.
Abnormality of dental enamel [hp:0000682]

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.

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.
Congenital pseudoarthrosis of the clavicle [hp:0006585]
Congenital pseudoarthrosis of the clavicle

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.
Congenital hypertrophy of left ventricle [hp:0005129]
Congenital hypertrophy of left ventricle

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.

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.

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.

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.

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.
Partial fusion of proximal row of carpal bones [hp:0005694]
Partial fusion of proximal row of carpal bones

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.

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.

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.
Prominent median palatal raphe [hp:0002708]

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.

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.

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.

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.

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.

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.

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.

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.

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.
Aplasia/Hypoplasia of the pubic bone [hp:0009104]

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.

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.

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.

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.

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.
Decreased T cell activation [hp:0005419]

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.
Small abnormally formed scapulae [hp:0006584]

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.
Nonprogressive encephalopathy [hp:0007030]

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.
Avascular necrosis of the capital femoral epiphysis [hp:0005743]
Avascular necrosis of the capital femoral epiphysis

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.
Antineutrophil antibody positivity [hp:0003453]

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.

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.

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.

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.
Midline facial capillary hemangioma [hp:0007601]

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.

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.
Elevated luteinizing hormone [hp:0011969]

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.
EEG with generalized polyspikes [hp:0012001]

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.

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.
Hypometric horizontal saccades [hp:0007975]

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.

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.
Ulnar metaphyseal irregularity [hp:0004042]

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.
Aplasia of the middle phalanges of the toes [hp:0100387]
Aplasia of the middle phalanges of the toes

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.

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.
Hoarse voice (caused by tumor impingement) [hp:0001613]
Hoarse voice (caused by tumor impingement)

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.

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.

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.

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.

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.
Primum atrial septal defect [hp:0010445]

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.

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.

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.

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.

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.
Sandwich appearance of vertebral bodies [hp:0004618]

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.

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.

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.
Generalized osteoporosis with pathologic fractures [hp:0005744]
Generalized osteoporosis with pathologic fractures

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.

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.
Increased circulating renin level [hp:0000848]

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.

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.
Periodic hypokalemic paresis [hp:0008153]

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.

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.

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.
Increased spinal bone density [hp:0004563]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Abnormally shaped carpal bones [hp:0006014]

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.

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.

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.

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.
Abnormal pelvis bone ossification [hp:0009106]

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.

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.

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.
Increased rate of premature chromosome condensation [hp:0003451]
Increased rate of premature chromosome condensation

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.
Abnormality of exocrine pancreas physiology [hp:0012092]
Abnormality of exocrine pancreas physiology

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.
Congenital foot contractures [hp:0005745]

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.

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.

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.
Tapering pointed ends of distal finger phalanges [hp:0006224]
Tapering pointed ends of distal finger phalanges

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.

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.
Beaking of vertebral bodies T12-L3 [hp:0004562]

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.

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.

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.

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.
Freckles in sun-exposed areas [hp:0007603]

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.

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.

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.
Recurrent vulvovaginal candidiasis [hp:0012204]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Abnormal ossification involving the femoral head and neck [hp:0009107]
Abnormal ossification involving the femoral head and neck

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.

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.
Progressive neurologic deterioration [hp:0002344]

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.

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.
Limitation of knee mobility [hp:0010501]

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.

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.

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.
Aplasia/Hypoplasia of the earlobes [hp:0009906]

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.
Depigmentation/hyperpigmentation of skin [hp:0007483]
Depigmentation/hyperpigmentation of skin

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.
Limited neck range of motion [hp:0000466]

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.

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.
Decreased renal tubular phosphate excretion [hp:0005572]
Decreased renal tubular phosphate excretion

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.
Generalized papillary lesions [hp:0007482]

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.

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.
Functional abnormality of the bladder [hp:0000009]

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.

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.
Ascending aortic dissection [hp:0004933]

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.

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.
Type 2 muscle fiber predominance [hp:0010602]

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.

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.

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.
Nonprogressive muscular atrophy [hp:0008964]

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.

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.

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.

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.

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.
Delayed phalangeal epiphyseal ossification [hp:0006016]
Delayed phalangeal epiphyseal ossification

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.
Abnormality of the carpal bones [hp:0001191]

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.

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.
Adrenocorticotropic hormone deficiency [hp:0011748]

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.

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.
Contractures of the joints of the lower limbs [hp:0005750]
Contractures of the joints of the lower limbs

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.
Aplasia/Hypoplasia involving the carpal bones [hp:0006502]
Aplasia/Hypoplasia involving the carpal bones

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.

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.
Recurrent gram-negative bacterial infections [hp:0005420]
Recurrent gram-negative bacterial infections

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.
T-cell acute lymphoblastic leukemias [hp:0006727]

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.

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.
Depletion of mitochondrial DNA in liver [hp:0006581]

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.

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.
Keratocystic odontogenic tumor [hp:0010603]

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.
Venous varicosities of celiac and mesenteric vessels [hp:0002626]
Venous varicosities of celiac and mesenteric vessels

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.
Exercise-induced muscle stiffness [hp:0008967]

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.

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.

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.
Unilateral vertebral artery hypoplasia [hp:0030323]

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.
Absence of subcutaneous fat [hp:0007485]

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.

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.
Intellectual disability, moderate [hp:0002342]

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.

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.

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.
Autosomal recessive inheritance [hp:0000007]

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.

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.
Non-acidotic proximal tubulopathy [hp:0005574]

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.
Decreased size of nerve terminals [hp:0003443]

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.
Wide tufts of distal phalanges [hp:0006095]

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.
Aplasia/Hypoplasia of the radius [hp:0006501]

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.
Decreased serum complement C3 [hp:0005421]

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.

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.
Unilateral hypoplasia of pectoralis major muscle [hp:0011959]
Unilateral hypoplasia of pectoralis major muscle

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.

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.
Right aortic arch with mirror image branching [hp:0002627]
Right aortic arch with mirror image branching

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.

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.
Reye syndrome-like episodes [hp:0006582]

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.
Asymptomatic hyperammonemia [hp:0008162]

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.
Mixed respiratory and metabolic acidosis [hp:0005967]
Mixed respiratory and metabolic acidosis

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.
Abnormality of bone mineral density [hp:0004348]

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.

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.
Congenital giant melanocytic nevus [hp:0005600]

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.
Joint contracture of the hand [hp:0009473]

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.

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.
Depigmented lesions of the retinal pigment epithelium [hp:0008017]
Depigmented lesions of the retinal pigment epithelium

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.
Unilateral vocal cord paralysis [hp:0008757]

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.
Normal pressure hydrocephalus [hp:0002343]

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.
Neoplasm of the gastrointestinal tract [hp:0007378]

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.

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.

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.

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.

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.
Juvenile myelomonocytic leukemia [hp:0012209]

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.

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.

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.
EMG: chronic denervation signs [hp:0003444]

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.
Abnormality of corneal stroma [hp:0011492]

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.

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.
Abnormality of female internal genitalia [hp:0000008]
Abnormality of female internal genitalia

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.

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.

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.

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.

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.
Aplasia cutis congenita over posterior parietal area [hp:0007590]
Aplasia cutis congenita over posterior parietal area

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.

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.
Reduced bone mineral density [hp:0004349]

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.

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.
Fatal liver failure in infancy [hp:0006583]

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.
Absent leukocyte alkaline phosphatase [hp:0008161]

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.

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.

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.
Everted lower lip vermilion [hp:0000232]

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.
Abnormalities of placenta or umbilical cord [hp:0001194]
Abnormalities of placenta or umbilical cord

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.

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.

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.

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.

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.

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.

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.

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.
Mild global developmental delay [hp:0011342]

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.
Dysfunctional alternative complement pathway [hp:0005423]
Dysfunctional alternative complement pathway

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.

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.
Gastrointestinal arteriovenous malformation [hp:0002629]
Gastrointestinal arteriovenous malformation

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.

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.

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.
Exocrine pancreatic insufficiency [hp:0001738]

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.

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.
Abnormality of urine catecholamine concentration [hp:0011281]
Abnormality of urine catecholamine concentration

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.

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.
Autosomal dominant inheritance [hp:0000006]

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.

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.
Increased proportion of HLA DR+ and CD57+ T cells [hp:0002853]
Increased proportion of HLA DR+ and CD57+ T cells

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.
Perimembranous ventricular septal defect [hp:0011682]
Perimembranous ventricular septal defect

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.

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.

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.

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.

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.
Warfarin-induced skin necrosis [hp:0001038]

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.
Focal seizures without impairment of consciousness or awareness [hp:0002349]
Focal seizures without impairment of consciousness or awareness

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.
Muscle hypertrophy of the lower extremities [hp:0008968]
Muscle hypertrophy of the lower extremities

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.
Abnormality of the oral cavity [hp:0000163]

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.
Absent specific antibody response [hp:0005424]

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.

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.

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.
Cerebellar hemangioblastoma [hp:0006880]

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.

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.
Symmetric peripheral demyelination [hp:0007262]

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.
Abnormality of the nasopharynx [hp:0001739]

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.
Abnormality of glycosphingolipid metabolism [hp:0004343]
Abnormality of glycosphingolipid metabolism

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.
Increased adipose tissue around the neck [hp:0000468]
Increased adipose tissue around the neck

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.
Severe postnatal growth retardation [hp:0008850]

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.

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.
Multicystic kidney dysplasia [hp:0000003]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Severe global developmental delay [hp:0011344]

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.
Recurrent sinopulmonary infections [hp:0005425]

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.
Adrenocorticotropic hormone excess [hp:0011749]

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.

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.

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.
Recurrent infection of the gastrointestinal tract [hp:0004798]
Recurrent infection of the gastrointestinal tract

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.
Arteriosclerosis of small cerebral arteries [hp:0004931]
Arteriosclerosis of small cerebral arteries

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.
Anterior creases of earlobe [hp:0009908]

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.

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.

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.

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.

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.

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.
Ulnar deviation of the hand or of fingers of the hand [hp:0001193]
Ulnar deviation of the hand or of fingers of the hand

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.
Increased number of CD4-/CD8- T cells expressing alpha/beta T-cell receptors [hp:0002851]
Increased number of CD4-/CD8- T cells expressing alpha/beta T-cell receptors

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.
Metacarpophalangeal joint hyperextensibility [hp:0006099]
Metacarpophalangeal joint hyperextensibility

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.
Angioid streaks of the retina [hp:0001102]

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.

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.
Focal segmental glomerulosclerosis [hp:0000097]

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.
Enlarged epiphysis of the middle phalanx of the 3rd finger [hp:0009324]
Enlarged epiphysis of the middle phalanx of the 3rd finger

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.
Increased intervertebral space [hp:0030320]

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.

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.
Numerous congenital melanocytic nevi [hp:0005603]

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.
Moderate global developmental delay [hp:0011343]

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.

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.
Abnormality of ganglioside metabolism [hp:0004345]

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.
Progressive night blindness [hp:0007675]

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.

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.

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.

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.
Persistent hyperplastic primary vitreous [hp:0007968]
Persistent hyperplastic primary vitreous

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.

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.

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.

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.
Decreased sensory nerve conduction velocity [hp:0003448]
Decreased sensory nerve conduction velocity

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.

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.
Increased renal tubular phosphate reabsorption [hp:0005571]
Increased renal tubular phosphate reabsorption

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.
Defective DNA repair after ultraviolet radiation damage [hp:0003079]
Defective DNA repair after ultraviolet radiation damage

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.
Abnormality of the pulmonary vasculature [hp:0004930]
Abnormality of the pulmonary vasculature

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.
Increased muscle glycogen content [hp:0009051]

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.

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.
Salt and pepper retinopathy [hp:0007814]

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.
Advanced ossification of carpal bones [hp:0004233]

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.
Cartilaginous ossification of nose [hp:0005275]

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.

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.

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.

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.

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.

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.
Abnormal metaphyseal vascular invasion [hp:0003562]

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.
Defective B cell differentiation [hp:0005357]

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.
Hyperpigmented nevi and streak [hp:0005606]

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.

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.

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.

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.
Streaks of hyperkeratosis along each finger onto the palm [hp:0007501]
Streaks of hyperkeratosis along each finger onto the palm

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.

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.

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.

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.

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.

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.

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.

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.
Decreased serum complement factor I [hp:0005356]

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.

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.

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.

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.

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.

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.
Large cafe-au-lait macules with irregular margins [hp:0005605]
Large cafe-au-lait macules with irregular margins

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.

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.

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.
Spontaneous esophageal perforation [hp:0005203]

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.
Drumstick terminal phalanges [hp:0006129]

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.

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.
Intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material [hp:0006916]
Intraaxonal accumulation of curvilinear autofluorescent lipopigment storage material

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.
Sex-limited autosomal dominant [hp:0001470]

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.

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.
Abnormality of the renal tubule [hp:0000091]

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.

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.

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.
Congenital palmoplantar keratodermia [hp:0007597]

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.
Decreased number of sweat glands [hp:0007500]

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.

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.
Abnormality of the humeroulnar joint [hp:0100745]

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.
Abnormality of the fontanelles or cranial sutures [hp:0000235]
Abnormality of the fontanelles or cranial sutures

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.
Absent nasal septal cartilage [hp:0005273]

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.

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.
Aplasia/Hypoplasia of the corpus callosum [hp:0007370]
Aplasia/Hypoplasia of the corpus callosum

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.
Distal lower limb muscle weakness [hp:0009053]

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.

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.

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.
Focal necrosis of right ventricular muscle cells [hp:0003338]
Focal necrosis of right ventricular muscle cells

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.
Herpetiform corneal ulceration [hp:0007812]

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.
Helicobacter pylori infection [hp:0005202]

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.

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.

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.

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.

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.

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.

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.
Abnormality of the inner ear [hp:0000359]

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.

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.

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.

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.
Bilateral single transverse palmar creases [hp:0007598]
Bilateral single transverse palmar creases

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.

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.

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.

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.

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.
Anomalous splenoportal venous system [hp:0005201]

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.

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.
Horizontal pendular nystagmus [hp:0007811]

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.
Pyrimidine-responsive megaloblastic anemia [hp:0003339]
Pyrimidine-responsive megaloblastic anemia

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.
Abnormality of cells of the megakaryocyte lineage [hp:0012143]
Abnormality of cells of the megakaryocyte lineage

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.
Birth length less than 3rd percentile [hp:0003561]

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.

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.

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.
Impaired distal vibration sensation [hp:0006886]

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.

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.

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.
Triangular shaped distal phalanges of the hand [hp:0009875]
Triangular shaped distal phalanges of the hand

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.

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.

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.
Periorbital hyperpigmentation [hp:0001106]

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.
Dermatan sulfate excretion in urine [hp:0008301]

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.
Abnormality of the tracheobronchial system [hp:0005607]
Abnormality of the tracheobronchial system

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.

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.

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.

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.

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.
Abnormality of prenatal development or birth [hp:0001197]
Abnormality of prenatal development or birth

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.
Generalized reticulate brown pigmentation [hp:0007599]
Generalized reticulate brown pigmentation

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.

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.

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.
Intellectual disability, progressive [hp:0006887]

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.

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.
Susceptibility to herpesvirus [hp:0005353]

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.

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.

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.
Generalized limb muscle atrophy [hp:0009055]

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.
Abnormal enchondral ossification [hp:0003336]

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.
Tubulointerstitial fibrosis [hp:0005576]

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.
Progressive hearing impairment [hp:0001730]

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.
Loss of subcutaneous adipose tissue from upper limbs [hp:0009056]
Loss of subcutaneous adipose tissue from upper limbs

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.

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.

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.
Subungual hyperkeratotic fragments [hp:0008410]

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.
Progressive hyperpigmentation [hp:0007505]

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.

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.

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.

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.

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.

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.

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.

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.
Dentinogenesis imperfecta limited to primary teeth [hp:0011060]
Dentinogenesis imperfecta limited to primary teeth

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.
Reduced prothrombin consumption [hp:0003337]

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.

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.

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.

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.
Aplasia/Hypoplastia of the eccrine sweat glands [hp:0007592]
Aplasia/Hypoplastia of the eccrine sweat glands

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.
Horizontal supranuclear gaze palsy [hp:0007817]

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.

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.

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.
Severe T-cell immunodeficiency [hp:0005352]

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.

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.
Aplasia/Hypoplasia of the 3rd toe [hp:0010331]

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.
Abnormality of the outer ear [hp:0000356]

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.

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.

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.
Aplasia/Hypoplasia of the phalanges of the hand [hp:0009767]
Aplasia/Hypoplasia of the phalanges of the hand

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.
Peripheral opacification of the cornea [hp:0008011]

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.
Malformation of the heart and great vessels [hp:0002564]
Malformation of the heart and great vessels

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.

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.

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.
Inability to walk by childhood/adolescence [hp:0006915]
Inability to walk by childhood/adolescence

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.

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.

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.

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.
Intellectual disability, borderline [hp:0006889]

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.
Abnormal cartilage collagen [hp:0008271]

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.

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.

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.
Elevated circulating catecholamine level [hp:0003334]
Elevated circulating catecholamine level

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.

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.
Decreased sweating due to autonomic dysfunction [hp:0007480]
Decreased sweating due to autonomic dysfunction

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.
Broad phalanges of the hand [hp:0009768]

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.

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.
Abnormality of the pancreas [hp:0001732]

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.
Increased muscle lipid content [hp:0009058]

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.

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.
Intellectual disability, mild [hp:0001256]

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.

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.

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.

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.

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.

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.
Impaired reabsorption of chloride [hp:0005579]

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.
Low gonadotropins (secondary hypogonadism) [hp:0003335]
Low gonadotropins (secondary hypogonadism)

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.

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.
Reduced quantity of Von Willebrand factor [hp:0012147]
Reduced quantity of Von Willebrand factor

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.

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.
Bullet-shaped phalanges of the hand [hp:0009769]

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.

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.

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.

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.

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.

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.
Cortical gyral simplification [hp:0009879]

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.

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.

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.
Neonatal short-trunk short stature [hp:0008857]

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.

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.
Long proximal phalanx of finger [hp:0006127]

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.

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.

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.
Degeneration of the striatum [hp:0040140]

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.

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.

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.

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.

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.

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.
Delayed closure of the anterior fontanelle [hp:0001476]
Delayed closure of the anterior fontanelle

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.

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.

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.

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.

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.
Calcific stippling of infantile cartilaginous skeleton [hp:0005841]
Calcific stippling of infantile cartilaginous skeleton

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.
Hypoplasia of proximal fibula [hp:0006442]

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.

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.
Prolonged brainstem auditory evoked potentials [hp:0004466]
Prolonged brainstem auditory evoked potentials

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.

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.

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.
Recurrent upper and lower respiratory tract infections [hp:0200117]
Recurrent upper and lower respiratory tract infections

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.
Widening of cervical spinal canal [hp:0004571]

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.
Diffuse mesangial sclerosis [hp:0001967]

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.

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.

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.

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.

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.

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.

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.

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.

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.
Impaired vibratory sensation [hp:0002495]

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.

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.
Male-limited autosomal dominant [hp:0001475]

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.

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.

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.
Conspicuously happy disposition [hp:0100024]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Decreased glucosephosphate isomerase activity [hp:0003568]
Decreased glucosephosphate isomerase activity

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.

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.

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.

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.

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.

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.

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.

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.
Type 1 fibers relatively smaller than type 2 fibers [hp:0003755]
Type 1 fibers relatively smaller than type 2 fibers

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.

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.
Progressive extrapyramidal movement disorder [hp:0007153]
Progressive extrapyramidal movement disorder

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.

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.

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.
Broad distal phalanges of all fingers [hp:0009880]

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.
Increased density of long bone diaphyses [hp:0006440]
Increased density of long bone diaphyses

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.

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.

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.

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.

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.

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.
Vocal cord paralysis (caused by tumor impingement) [hp:0001606]
Vocal cord paralysis (caused by tumor impingement)

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.

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.

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.

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.
Elevated leukocyte alkaline phosphatase [hp:0008318]

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.

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.
Compensatory chin elevation [hp:0001477]

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.

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.

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.
Aplasia/Hypoplasia of metatarsal bones [hp:0001964]

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.

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.

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.
Thickened superior cerebellar peduncle [hp:0002404]

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.
Atrophy of the dentate nucleus [hp:0007047]

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.
Short distal phalanx of finger [hp:0009882]

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.

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.

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.

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.
Patchy hypo- and hyperpigmentation [hp:0007509]

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.

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.
Premature calcification of mitral annulus [hp:0005136]
Premature calcification of mitral annulus

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.
Abnormality of chromosome segregation [hp:0002916]

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.

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.
Absent brainstem auditory responses [hp:0004463]

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.

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.

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.

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.
Malabsorption of Vitamin B12 [hp:0200118]

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.
Duplication of the distal phalanx of hand [hp:0009883]
Duplication of the distal phalanx of hand

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.

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.

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.

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.
Symphalangism affecting the phalanges of the hand [hp:0009773]
Symphalangism affecting the phalanges of the hand

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.
Transient neonatal diabetes mellitus [hp:0008255]

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.

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.
Abnormal speech discrimination [hp:0001963]

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.

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.
Abnormality of the corticospinal tract [hp:0002492]

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.
Aplasia/Hypoplasia of the colon [hp:0100811]

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.
Recurrent lower respiratory tract infections [hp:0002783]
Recurrent lower respiratory tract infections

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.

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.
Elevated erythrocyte sedimentation rate [hp:0003565]

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.

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.
Thin glomerular basement membrane [hp:0012577]

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.
Prolonged bleeding after dental extraction [hp:0006298]
Prolonged bleeding after dental extraction

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.

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.
Decreased circulating renin level [hp:0003351]

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.

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.

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.

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.
Agenesis of maxillary lateral incisor [hp:0000690]

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.
Tapered distal phalanges of finger [hp:0009884]

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.
Patchy sclerosis of finger phalanx [hp:0009772]

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.

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.
Spasticity of facial muscles [hp:0002491]

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.

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.
EEG with irregular generalized spike and wave complexes [hp:0001326]
EEG with irregular generalized spike and wave complexes

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.

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.

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.

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.
Short distal phalanx of the 3rd finger [hp:0004180]

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.

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.

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.
Abnormal mitochondria in muscle tissue [hp:0008316]

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.

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.
Abnormality of urine homeostasis [hp:0003110]

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.
Folate-dependent fragile site at Xq28 [hp:0003564]

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.

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.

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.
Hypoplasia of dental enamel [hp:0006297]

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.

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.
Absence of the pulmonary valve [hp:0005134]

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.

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.
Abnormality of cells of the lymphoid lineage [hp:0012140]
Abnormality of cells of the lymphoid lineage

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.

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.

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.

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.
Osteolytic defects of the phalanges of the hand [hp:0009771]
Osteolytic defects of the phalanges of the hand

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.

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.
Anterolateral radial head dislocation [hp:0005050]

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.

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.
Impaired epinephrine-induced platelet aggregation [hp:0008148]
Impaired epinephrine-induced platelet aggregation

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.
Decreased plasma free carnitine [hp:0008315]

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.

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.

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.
Abnormal rapid eye movement (REM) sleep [hp:0002494]

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.

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.

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.

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.

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.
Aplasia cutis congenita on trunk or limbs [hp:0007589]
Aplasia cutis congenita on trunk or limbs

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.

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.

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.

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.

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.
Limited mobility of proximal interphalangeal joint [hp:0006217]
Limited mobility of proximal interphalangeal joint

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.
Anomalous tracheal cartilage [hp:0004468]

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.

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.
Right ventricular dilatation [hp:0005133]

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.
Propionyl-CoA carboxylase deficiency [hp:0003353]

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.

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.
Hypoplasia of lymphatic vessels [hp:0003759]

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.

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.
Reduced subcutaneous adipose tissue [hp:0003758]

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.

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.
Decreased activity of mitochondrial complex II [hp:0008314]
Decreased activity of mitochondrial complex II

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.

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.

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.
Hypokalemic metabolic alkalosis [hp:0001960]

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.
Upper motor neuron dysfunction [hp:0002493]

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.

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.

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.

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.
Reticular hyperpigmentation [hp:0007588]

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.
Abnormality of the optic nerve [hp:0000587]

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.

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.
Specific learning disability [hp:0001328]

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.

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.
Abnormality of hair texture [hp:0010719]

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.

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.
Increased serum prostaglandin E2 [hp:0003566]

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.

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.
Acute promyelocytic leukemia [hp:0004836]

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.
Progressive bifocal chorioretinal atrophy [hp:0007810]
Progressive bifocal chorioretinal atrophy

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.

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.
Pancreatic squamous cell carcinoma [hp:0012142]

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.

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.

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.

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.

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.
Endopolyploidy on chromosome studies of bone marrow [hp:0003352]
Endopolyploidy on chromosome studies of bone marrow

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.

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.

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.

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.
Chronic lymphocytic meningitis [hp:0007041]

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.
Recurrent bacterial skin infections [hp:0005406]

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.
Slender distal phalanx of finger [hp:0012296]

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.

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.

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.
Degenerative vitreoretinopathy [hp:0007964]

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.

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.
Decreased glomerular filtration rate [hp:0012213]

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.
Metopic suture patent to nasal root [hp:0005495]

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.
Female pseudohermaphroditism [hp:0010458]

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.

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.
Tortuosity of conjunctival vessels [hp:0000503]

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.

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.

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.

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.

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.
Absent distal interphalangeal creases [hp:0001032]

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.

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.
Triangular epiphysis of the middle phalanx of the 2nd finger [hp:0009523]
Triangular epiphysis of the middle phalanx of the 2nd finger

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.
Adrenocorticotropin (ACTH) receptor (ACTHR) defect [hp:0008259]
Adrenocorticotropin (ACTH) receptor (ACTHR) defect

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.

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.

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.

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.
IgA deposition in the glomerulus [hp:0000794]

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.
Low-to-normal blood pressure [hp:0002632]

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.

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.
Long eyelashes in irregular rows [hp:0007740]

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.
Slender proximal phalanx of finger [hp:0012297]

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.

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.
Single interphalangeal crease of fifth finger [hp:0006216]
Single interphalangeal crease of fifth finger

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.
Absence of visual evoked potentials [hp:0007965]

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.

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.

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.

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.

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.
Cleft at the superior portion of the pinna [hp:0008537]
Cleft at the superior portion of the pinna

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.
Abnormality of the conjunctiva [hp:0000502]

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.

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.
Acute tubulointerstitial nephritis [hp:0004729]

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.

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.

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.

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.
Primary adrenal insufficiency [hp:0008207]

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.
Elevated hepatic transaminases [hp:0002910]

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.

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.

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.

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.

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.

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.

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.
Thin proximal phalanges with broad epiphyses of the hand [hp:0006213]
Thin proximal phalanges with broad epiphyses of the hand

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.

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.

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.

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.
Choroidoretinal degeneration [hp:0200065]

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.

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.
Elevated 8-dehydrocholesterol [hp:0003462]

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.

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.
Abnormality of the nasolacrimal system [hp:0000614]

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.

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.

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.
Ivory epiphyses of the phalanges of the hand [hp:0010234]
Ivory epiphyses of the phalanges of the hand

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.

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.

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.
Increased number of peripheral CD3+ T cells [hp:0002845]
Increased number of peripheral CD3+ T cells

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.

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.

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.

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.
Flattening of the talar dome [hp:0008144]

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.

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.

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.

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.
Upslanted palpebral fissure [hp:0000582]

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.

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.

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.
Neonatal insulin-dependent diabetes mellitus [hp:0000857]
Neonatal insulin-dependent diabetes mellitus

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.

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.
Sclerotic vertebral endplates [hp:0004576]

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.
Increased urinary O-linked sialopeptides [hp:0003461]
Increased urinary O-linked sialopeptides

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.

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.
Cervical vertebral fusion (C2/C3) [hp:0004602]

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.
Midline skin dimples over anterior/posterior fontanelles [hp:0005498]
Midline skin dimples over anterior/posterior fontanelles

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.

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.
Long distal phalanx of finger [hp:0012299]

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.
Delayed eruption of permanent teeth [hp:0000696]

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.

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.
Facial flushing after alcohol intake [hp:0001033]

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.
Impaired renal concentrating ability [hp:0004727]

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.
Teleangiectasia of the skin [hp:0100585]

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.
Increased urinary potassium [hp:0003081]

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.
Congenital nonbullous ichthyosiform erythroderma [hp:0007479]
Congenital nonbullous ichthyosiform erythroderma

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.
Recurrent upper respiratory tract infections [hp:0002788]
Recurrent upper respiratory tract infections

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.

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.

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.

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.
Insulin-dependent but ketosis-resistant diabetes [hp:0008205]
Insulin-dependent but ketosis-resistant diabetes

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.
Congenital adrenal hyperplasia [hp:0008258]

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.

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.

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.

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.

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.

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.

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.
Impaired memory B-cell generation [hp:0002847]

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.

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.
Abnormal cholesterol homeostasis [hp:0003464]

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.
Recurrent spontaneous abortion [hp:0200067]

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.

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.

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.
Anterior beaking of lower thoracic vertebrae [hp:0004607]
Anterior beaking of lower thoracic vertebrae

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.
Fluctuations in consciousness [hp:0007159]

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.

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.

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.

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.

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.

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.

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.

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.
L-2-hydroxyglutaric aciduria [hp:0040144]

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.

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.

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.

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.

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.

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.
Fractures of the long bones [hp:0003084]

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.
Specific anti-polysaccharide antibody deficiency [hp:0002848]
Specific anti-polysaccharide antibody deficiency

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.
Delayed calcaneal ossification [hp:0008142]

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.
Spinal stenosis with reduced interpedicular distance [hp:0005733]
Spinal stenosis with reduced interpedicular distance

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.
Irregular ossification at anterior rib ends [hp:0006598]
Irregular ossification at anterior rib ends

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.
Increased extraneuronal autofluorescent lipopigment [hp:0003463]
Increased extraneuronal autofluorescent lipopigment

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.

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.

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.
Rarefaction of retinal pigmentation [hp:0007961]

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.

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.

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.

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.
Markedly reduced T cell function [hp:0005409]

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.

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.
Midline brain calcifications [hp:0007045]

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.
Anteriorly placed odontoid process [hp:0004608]

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.

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.

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.
Abnormality of the preputium [hp:0100587]

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.

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.

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.

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.

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.
Absence of lymph node germinal center [hp:0002849]

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.
Paradoxical increased cortisol secretion on dexamethasone suppression test [hp:0003466]
Paradoxical increased cortisol secretion on dexamethasone suppression test

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.
Thickening of the glomerular basement membrane [hp:0004722]
Thickening of the glomerular basement membrane

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.

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.

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.

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.

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.
Absent vertebral body mineralization [hp:0004605]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Mild postnatal growth retardation [hp:0001530]

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.

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.
Cone-shaped epiphyses of the phalanges of the hand [hp:0010230]
Cone-shaped epiphyses of the phalanges of the hand

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.

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.

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.

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.
L-2-hydroxyglutaric acidemia [hp:0040147]

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.
Aplasia/hypoplasia of the humerus [hp:0006507]

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.
Macroreticular retinal dystrophy [hp:0007963]

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.

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.
Decreased number of CD4+ T cells [hp:0005407]

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.

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.

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.

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.
Membranoproliferative glomerulonephritis [hp:0000793]
Membranoproliferative glomerulonephritis

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.
Unossified vertebral bodies [hp:0004606]

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.
Asymmetric limb muscle stiffness [hp:0007156]

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.

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.
Increased muscle fatiguability [hp:0003750]

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.

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.

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.

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.
Cerebellar vermis hypoplasia [hp:0001320]

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.

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.
Secundum atrial septal defect [hp:0001684]

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.
Failure to thrive in infancy [hp:0001531]

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.

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.
Abnormality of the aryepiglottic fold [hp:0008744]

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.

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.
Crusting erythematous dermatitis [hp:0007473]

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.
Bifid distal phalanx of toe [hp:0001853]

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.

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.

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.

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.
Radial deviation of the hand [hp:0009486]

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.

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.
Failure to thrive secondary to recurrent infections [hp:0008866]
Failure to thrive secondary to recurrent infections

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.

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.

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.

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.

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.
Elevated serum transaminases during infections [hp:0008150]
Elevated serum transaminases during infections

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.
Hereditary nonpolyposis colorectal carcinoma [hp:0006716]
Hereditary nonpolyposis colorectal carcinoma

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.

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.

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.
Elevated long chain fatty acids [hp:0003455]

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.

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.
Respiratory tract infection [hp:0011947]

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.

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.
Atrophy/Degeneration affecting the brainstem [hp:0007366]
Atrophy/Degeneration affecting the brainstem

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.
Headache (with pheochromocytoma) [hp:0002331]

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.

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.

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.

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.
Primary hyperparathyroidism [hp:0008200]

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.

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.

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.

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.
Pulmonary capillary hemangiomatosis [hp:0005954]

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.

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.

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.
Decreased numbers of nephrons [hp:0005563]

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.
Low urinary cyclic AMP response to PTH administration [hp:0003456]
Low urinary cyclic AMP response to PTH administration

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.

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.
Central adrenal insufficiency [hp:0011734]

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.

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.
Inlet ventricular septal defect [hp:0011622]

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.

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.

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.

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.
Cystoid macular degeneration [hp:0008028]

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.

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.

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.

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.
Aplasia/Hypoplasia of the sternum [hp:0006714]

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.

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.

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.

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.

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.

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.
Heparan sulfate excretion in urine [hp:0002159]

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.
Periarticular subcutaneous nodules [hp:0007470]

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.

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.

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.

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.

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.

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.

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.

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.

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.
Muscular ventricular septal defect [hp:0011623]

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.

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.

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.
Metaphyseal cupping of metacarpals [hp:0006028]

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.
Arnold-Chiari type I malformation [hp:0007099]

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.

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.

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.

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.
Glomus tympanicum paraganglioma [hp:0006715]

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.

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.

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.
Rib segmentation abnormalities [hp:0006655]

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.
Delayed peripheral myelination [hp:0011401]

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.
Anomalous rib insertion to vertebrae [hp:0006593]

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.

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.
Decreased pulmonary function [hp:0005952]

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.
Superficial thrombophlebitis [hp:0002638]

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.
EMG: myopathic abnormalities [hp:0003458]

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.
Impaired temperature sensation [hp:0010829]

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.
Abnormality of bone marrow cell morphology [hp:0005561]
Abnormality of bone marrow cell morphology

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.

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.
Intraalveolar nodular calcifications [hp:0006514]

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.
Short chordae tendineae of the mitral valve [hp:0011580]
Short chordae tendineae of the mitral valve

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.

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.

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.
Abnormality of the cerebellar vermis [hp:0002334]

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.

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.

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.
Longitudinal vaginal septum [hp:0008740]

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.

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.

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.

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.
Accelerated atherosclerosis [hp:0004943]

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.

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.
Polyclonal elevation of IgM [hp:0003459]

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.
Short distal phalanx of toe [hp:0001857]

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.
Demyelinating sensory neuropathy [hp:0011402]

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.
Accelerated skeletal maturation [hp:0005616]

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.

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.

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.

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.
Absent rod-and cone-mediated responses on ERG [hp:0007688]
Absent rod-and cone-mediated responses on ERG

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.

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.
Agenesis of cerebellar vermis [hp:0002335]

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.
Precocious puberty with Sertoli cell tumor [hp:0008204]
Precocious puberty with Sertoli cell tumor

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.
Skin dimple over apex of long bone angulation [hp:0001024]
Skin dimple over apex of long bone angulation

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.

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.

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.

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.
Enlarged epiphysis of the proximal phalanx of the 2nd finger [hp:0009527]
Enlarged epiphysis of the proximal phalanx of the 2nd finger

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.
Small epiphyses of the phalanges of the hand [hp:0010236]
Small epiphyses of the phalanges of the hand

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Posterior synechiae of the anterior chamber [hp:0011484]
Posterior synechiae of the anterior chamber

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.

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.

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.

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.

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.
Nonepidermolytic palmoplantar keratoderma [hp:0007404]
Nonepidermolytic palmoplantar keratoderma

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.

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.
Pulsatile tinnitus (tympanic paraganglioma) [hp:0000361]
Pulsatile tinnitus (tympanic paraganglioma)

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.

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.

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.
Recurrent Burkholderia cepacia infections [hp:0002842]
Recurrent Burkholderia cepacia infections

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.
Velopharyngeal insufficiency [hp:0000220]

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.
Congenital bullous ichthyosiform erythroderma [hp:0007475]
Congenital bullous ichthyosiform erythroderma

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.

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.

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.
Aplasia of the middle phalanx of the hand [hp:0010239]
Aplasia of the middle phalanx of the hand

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.
Stippled calcification in carpal bones [hp:0004241]

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.

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.

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.
Abnormal pupillary function [hp:0007686]

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.

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.

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.
Beaking of vertebral bodies [hp:0004568]

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.

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.
Hypoplasia of the epiglottis [hp:0005349]

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.

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.
Childhood onset short-limb short stature [hp:0011405]
Childhood onset short-limb short stature

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.

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.

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.
Ulnar deviation of the hand [hp:0009487]

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.

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.
Hypertrophy of skin of soles [hp:0007403]

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.

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.
Anhidrotic ectodermal dysplasia [hp:0007476]

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.
Recurrent fungal infections [hp:0002841]

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.
Generalized arterial calcification [hp:0004940]

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.

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.
Optic atrophy from cranial nerve compression [hp:0007958]
Optic atrophy from cranial nerve compression

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.

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.
Internally rotated shoulders [hp:0006659]

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.
Aplasia/hypoplasia of the femur [hp:0005613]

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.
Peripheral retinal avascularization [hp:0007685]

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.
Chronic obstructive pulmonary disease [hp:0006510]

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.

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.

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.

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.

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.

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.

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.
Irregular femoral epiphysis [hp:0006361]

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.
Progressive retinal degeneration [hp:0007893]

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.
Symmetrical progressive peripheral demyelination [hp:0006873]
Symmetrical progressive peripheral demyelination

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.

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.

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.

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.
Increased axial globe length [hp:0007800]

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.

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.

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.

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.

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.
Infancy onset short-trunk short stature [hp:0011406]

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.

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.

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.
Abnormality of corneal endothelium [hp:0011488]

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.
Hypopigmentation of the fundus [hp:0007894]

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.
Abnormality of ulnar metaphysis [hp:0004039]

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.
Progressive cone degeneration [hp:0008020]

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.

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.

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.
Maternal hyperphenylalaninemia [hp:0100610]

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.
Scapulohumeral muscular dystrophy [hp:0008970]

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.
Numerous pigmented freckles [hp:0007587]

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.

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.
Noninflammatory macular atrophy [hp:0007401]

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.

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.

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.
Edema of the dorsum of hands [hp:0007514]

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.
Abnormality of hair pigmentation [hp:0009887]

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.

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.
Atypical or prolonged hepatitis [hp:0200122]

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.
Exostosis of the external auditory canal [hp:0004459]
Exostosis of the external auditory canal

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.

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.

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.

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.
Increased corneal thickness [hp:0011487]

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.

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.
Positive regitine blocking test [hp:0003574]

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.
Pulmonary lymphangiomyomatosis [hp:0012798]

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.

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.

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.
Aplasia/Hypoplasia of the cerebellum [hp:0007360]

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.
Irregular hyperpigmentation [hp:0007400]

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.

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.

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.

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.

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.
Hypoglycemic encephalopathy [hp:0006929]

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.
Triangular epiphysis of the middle phalanx of the 3rd finger [hp:0009331]
Triangular epiphysis of the middle phalanx of the 3rd finger

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.

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.
Generalized hypopigmentation [hp:0007513]

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.
Hypoplasia of the lacrimal puncta [hp:0007892]

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.

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.

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.

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.

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.

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.
Impaired FSH and LH secretion [hp:0003295]

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.

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.

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.
Increased intracellular sodium [hp:0003575]

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.

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.
Abnormality of the carotid arteries [hp:0005344]

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.

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.
Hyperextensibility of the finger joints [hp:0001187]

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.

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.
Skin fragility with non-scarring blistering [hp:0007585]
Skin fragility with non-scarring blistering

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.

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.
Spinal cord posterior columns myelin loss [hp:0008311]
Spinal cord posterior columns myelin loss

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.

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.
Congenital talipes calcaneovalgus [hp:0005850]

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.
Chronic hepatitis due to cryptospridium infection [hp:0200124]
Chronic hepatitis due to cryptospridium infection

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.
Thickening of the lateral border of the scapula [hp:0006650]
Thickening of the lateral border of the scapula

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.

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.

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.
Abnormality of the upper urinary tract [hp:0010935]

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.
Increased cup-to-disc ratio [hp:0012796]

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.

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.
Subperiosteal erosions due to secondary hyperparathyroidism [hp:0003106]
Subperiosteal erosions due to secondary hyperparathyroidism

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.

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.

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.

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.

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.

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.

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.
Lack of subcutaneous fatty tissue [hp:0007519]

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.

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.

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.
Punctate vertebral calcifications [hp:0008420]

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.
Horizontal opticokinetic nystagmus [hp:0008026]

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.
Abnormality of the mesentery [hp:0100016]

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.

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.

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.
Severe demyelination of the white matter [hp:0007258]
Severe demyelination of the white matter

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.

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.

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.
Mitochondrial respiratory chain defects [hp:0200125]

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.

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.

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.
Impaired lymphocyte transformation with phytohemagglutinin [hp:0003347]
Impaired lymphocyte transformation with phytohemagglutinin

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.
Abnormality of cells of the granulocytic lineage [hp:0012135]
Abnormality of cells of the granulocytic lineage

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.

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.

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.

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.

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.
Abnormality of cholesterol metabolism [hp:0003107]

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.
Abnormality of the optic disc [hp:0012795]

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.

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.
Gastrointestinal angiodysplasia [hp:0000471]

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.

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.

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.

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.
Telangiectasia macularis eruptiva perstans [hp:0007583]
Telangiectasia macularis eruptiva perstans

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.

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.
Exercise-induced rhabdomyolysis [hp:0009045]

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.

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.

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.

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.

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.

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.

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.

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.
Autonomic bladder dysfunction [hp:0005341]

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.
Absence of renal corticomedullary differentiation [hp:0005564]
Absence of renal corticomedullary differentiation

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.
Conjugated hyperbilirubinemia [hp:0002908]

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.

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.
Molybdenum cofactor deficiency [hp:0003570]

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.
Cerebral arteriovenous malformation [hp:0002408]

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.
Cystic lesions of the pinnae [hp:0010723]

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.

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.

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.

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.

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.

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.
Congenital nuclear cataract [hp:0008024]

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.

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.

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.

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.

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.

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.
Mildly reduced visual acuity [hp:0007739]

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.
Exaggerated startle response [hp:0002267]

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.

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.
Low cholesterol esterification rates [hp:0003349]

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.
Reduced renal corticomedullary differentiation [hp:0005565]
Reduced renal corticomedullary differentiation

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.
Spastic/hyperactive bladder [hp:0005340]

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.
Varus deformity of humeral neck [hp:0006362]

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.

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.
Protuberances at ends of long bones [hp:0003105]

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.

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.

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.
Cartilaginous ossification of larynx [hp:0008747]

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.
Tall lumbar vertebral bodies [hp:0008421]

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.
Recurrent urinary tract infections [hp:0000010]

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.

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.
Benign gastrointestinal tract tumors [hp:0006719]

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.

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.
Decreased activity of mitochondrial respiratory chain [hp:0008972]
Decreased activity of mitochondrial respiratory chain

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.

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.

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.

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.
Low-set, posteriorly rotated ears [hp:0000368]

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.

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.

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.
Impaired thrombin-induced platelet aggregation [hp:0011872]
Impaired thrombin-induced platelet aggregation

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.

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.

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.
Neoplasm of the parathyroid gland [hp:0100733]

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.

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.

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.

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.

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.

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.

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.
Frontoparietal polymicrogyria [hp:0007095]

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.

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.
Cerebral cortical neurodegeneration [hp:0006964]

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.

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.

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.
High maternal serum alpha-fetoprotein [hp:0011432]

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.

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.
Neuronal loss in basal ganglia [hp:0200147]

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.
Cortically dense long tubular bones [hp:0006415]

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.
Aplasia cutis congenita over the scalp vertex [hp:0004471]
Aplasia cutis congenita over the scalp vertex

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.
Abnormal isoelectric focusing of serum transferrin [hp:0003160]
Abnormal isoelectric focusing of serum transferrin

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.
Abnormality of the gallbladder [hp:0005264]

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.

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.
High-frequency sensorineural hearing impairment [hp:0001757]
High-frequency sensorineural hearing impairment

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.

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.

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.

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.

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.
Neonatal unconjugated hyperbilirubinemia [hp:0008176]
Neonatal unconjugated hyperbilirubinemia

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.
Abnormality of the hairline [hp:0009553]

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.

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.

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.
Progressive external ophthalmoplegia [hp:0000590]

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.

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.

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.
Acute necrotizing encephalopathy [hp:0006965]

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.
Abnormality of the first metatarsal bone [hp:0010054]
Abnormality of the first metatarsal bone

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.

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.

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.

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.
4-Hydroxyphenylpyruvic aciduria [hp:0003161]

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.

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.

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.

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.

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.

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.

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.

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.
Myotonia with warm-up phenomenon [hp:0003740]

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.

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.

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.
Reversed usual vertebral column curves [hp:0008433]

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.
Projection of scalp hair onto lateral cheek [hp:0009554]
Projection of scalp hair onto lateral cheek

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Vertical supranuclear gaze palsy [hp:0000511]

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.
Abnormality of vertebral epiphysis morphology [hp:0100734]
Abnormality of vertebral epiphysis morphology

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.

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.

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.
Congenital muscular dystrophy [hp:0003741]

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.

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.

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.

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.
Hypoplastic cervical vertebrae [hp:0008434]

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.

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.

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.
Vitreoretinal abnormalities [hp:0007773]

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.

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.
Hypoplasia of the optic tract [hp:0007096]

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.
Persistent open anterior fontanelle [hp:0004474]

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.

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.

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.

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.

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.
Elevated urinary delta-aminolevulinic acid [hp:0003163]
Elevated urinary delta-aminolevulinic acid

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.

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.

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.

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.

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.

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.

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.
Limitation of joint mobility [hp:0001376]

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.

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.

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.
Abnormality of the musculature [hp:0003011]

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.
Hypothalamic gonadotropin-releasing hormone (GNRH) deficiency [hp:0003164]
Hypothalamic gonadotropin-releasing hormone (GNRH) deficiency

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.
Prolonged G2 phase of cell cycle [hp:0003214]

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.
Punctate vasculitis skin lesions [hp:0200030]

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.
Chondroitin sulfate excretion in urine [hp:0012070]

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.
Hypoplasia of the ciliary body [hp:0007774]

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.

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.

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.
Muscular hypotonia of the trunk [hp:0008936]

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.
Deviation of the 5th finger [hp:0009179]

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.

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.

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.

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.

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.

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.
Increased mean platelet volume [hp:0011877]

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.

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.
Elevated circulating parathyroid hormone (PTH) level [hp:0003165]
Elevated circulating parathyroid hormone (PTH) level

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.

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.
Abnormality of the soft palate [hp:0100736]

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.
Deficient excision of UV-induced pyrimidine dimers in DNA [hp:0003213]
Deficient excision of UV-induced pyrimidine dimers in DNA

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.

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.

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.

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.

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.
Reticulate pigmentation of oral mucosa [hp:0012788]

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.
EEG with generalized slow activity [hp:0010845]

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.

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.

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.
Abnormality of the anterior chamber [hp:0000593]

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.
Abnormal atrioventricular conduction [hp:0005150]

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.

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.

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.
Median cleft lip and palate [hp:0008501]

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.
Telangiectases of the cheeks [hp:0007421]

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.

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.

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.

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.

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.

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.

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.
CSF lymphocytic pleiocytosis [hp:0200149]

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.
Slow saccadic eye movements [hp:0000514]

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.

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.

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.
Fifth metacarpal with ulnar notch [hp:0005900]

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.
Large clumps of pigment irregularly distributed along hair shaft [hp:0004527]
Large clumps of pigment irregularly distributed along hair shaft

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.
Generalized amyloid deposition [hp:0003216]

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.

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.

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.
Preductal coarctation of the aorta [hp:0005151]

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.
Decreased adipose tissue around neck [hp:0005995]

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.
Underfolded superior helices [hp:0008583]

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.
Proximal/middle symphalangism of 5th finger [hp:0009177]
Proximal/middle symphalangism of 5th finger

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.

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.
Anterior beaking of lumbar vertebrae [hp:0008430]

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.

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.

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.
Hypoplasia of the capital femoral epiphysis [hp:0003090]
Hypoplasia of the capital femoral epiphysis

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.

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.

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.

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.

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.

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.

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.

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.
Abnormal liver function tests during pregnancy [hp:0200148]
Abnormal liver function tests during pregnancy

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.

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.

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.

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.
Abnormality of the pulmonary veins [hp:0011718]

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.
Chronic recurrent multifocal osteomyelitis [hp:0005901]
Chronic recurrent multifocal osteomyelitis

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.

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.

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.

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.
Posterior leukoencephalopathy [hp:0006859]

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.

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.

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.
Delayed gross motor development [hp:0002194]

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.
Progressive pulmonary function impairment [hp:0006520]
Progressive pulmonary function impairment

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.
Neovascularization of peripheral and posterior retina [hp:0007778]
Neovascularization of peripheral and posterior retina

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.

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.

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.
Proximal renal tubular acidosis [hp:0002049]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Elevated imprint of the transverse sinuses [hp:0000930]
Elevated imprint of the transverse sinuses

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.
Cutaneous syndactyly of toes [hp:0010621]

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.

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.

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.
Costal cartilage calcification [hp:0006646]

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.
Dysgenesis of the cerebellar vermis [hp:0002195]

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.

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.

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.

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.

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.
Anterior segment of eye aplasia [hp:0007779]

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.
Hyperreflexia in upper limbs [hp:0007350]

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.

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.

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.

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.
3-4 finger cutaneous syndactyly [hp:0011939]

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.

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.

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.
Defect in the atrial septum [hp:0001631]

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.

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.

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.

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.
Autoimmune thrombocytopenia [hp:0001973]

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.

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.

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.

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.
Bulging of the costochondral junction [hp:0000893]

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.

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.
Thinning and bulging of the posterior fossa bones [hp:0000931]
Thinning and bulging of the posterior fossa bones

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.

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.
Late onset congenital glaucoma [hp:0008041]

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.
Increased red cell osmotic fragility [hp:0005502]

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.
Abnormality of the abdominal organs [hp:0002012]

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.

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.
Recurrent infections due to aspiration [hp:0004891]

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.
Irregular, rachitic-like metaphyses [hp:0005042]

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.

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.

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.

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.

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.
Cystic retinal degeneration [hp:0007667]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Joint swelling onset late infancy [hp:0005833]

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.
Pseudobulbar behavioral symptoms [hp:0002193]

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.
Pelvic girdle muscle weakness [hp:0003749]

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.
Morphological abnormality of the central nervous system [hp:0002011]
Morphological abnormality of the central nervous system

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.
Irregular capital femoral epiphysis [hp:0005041]

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.

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.
Giant melanosomes in melanocytes [hp:0005592]

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.

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.

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.

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.

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.

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.

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.
Impaired pursuit initiation and maintenance [hp:0007668]
Impaired pursuit initiation and maintenance

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.
X-linked recessive inheritance [hp:0001419]

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.

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.
Decreased platelet glycoprotein IIb-IIIa [hp:0001975]
Decreased platelet glycoprotein IIb-IIIa

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.

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.

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.

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.
Neoplasm of the skeletal system [hp:0010622]

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.

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.

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.
Mild neurosensory hearing impairment [hp:0008587]

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.

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.
Tracheobronchial leiomyomatosis [hp:0006524]

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.

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.

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.
Decreased plasma total carnitine [hp:0011936]

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.

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.

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.

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.

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.

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.

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.

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.
Chorioretinal hypopigmentation or hyperpigmentation [hp:0007661]
Chorioretinal hypopigmentation or hyperpigmentation

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.
Chromosomal breakage induced by ionizing radiation [hp:0010997]
Chromosomal breakage induced by ionizing radiation

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.

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.

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.

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.
Megaloblastic erythroid hyperplasia [hp:0200143]

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.
Slit-like opening of the exterior auditory meatus [hp:0008588]
Slit-like opening of the exterior auditory meatus

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.
Reticulated skin pigmentation [hp:0007427]

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.

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.

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.

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.
Mild intrauterine growth retardation [hp:0008883]

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.

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.

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.
Amyotrophic lateral sclerosis [hp:0007354]

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.
Reduced antithrombin III activity [hp:0001976]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Abnormality of B cell physiology [hp:0005372]

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.

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.
Facial telangiectasia in butterfly midface distribution [hp:0005598]
Facial telangiectasia in butterfly midface distribution

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.

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.

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.

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.
Large sternal ossification centers [hp:0006642]

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.

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.

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.

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.
Elevated pulmonary artery pressure [hp:0004890]

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.
Thickened cortex of long bones [hp:0000935]

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.
Aplastic/hypoplastic toenail [hp:0010624]

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.

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.
Telangiectasia of the oral mucosa [hp:0007428]

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.

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.

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.

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.

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.

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.

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.

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.
Atypical nevi (>5mm with irregular edge and pigmentation) [hp:0001062]
Atypical nevi (>5mm with irregular edge and pigmentation)

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.
Fused sternal ossification centers [hp:0006643]

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.
Absent fourth finger distal interphalangeal crease [hp:0005780]
Absent fourth finger distal interphalangeal crease

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.

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.
Extramedullary hematopoiesis [hp:0001978]

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.

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.
Anterior pituitary hypoplasia [hp:0010627]

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.

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.

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.

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.

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.
Chronic myelogenous leukemia [hp:0005506]

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.

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.
Abnormality of the posterior cranial fossa [hp:0000932]
Abnormality of the posterior cranial fossa

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.

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.

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.
Genetic anticipation with paternal anticipation bias [hp:0003744]
Genetic anticipation with paternal anticipation bias

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.
Anomalous pulmonary venous return [hp:0010772]

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.

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.

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.

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.

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.

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.
Contractures of the large joints [hp:0005781]

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.
Lymphoid interstitial pneumonia [hp:0006527]

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.

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.

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.

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.

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.
Diaphyseal cortical sclerosis [hp:0005045]

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.

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.

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.

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.
Anterior pituitary agenesis [hp:0010626]

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.
Posterior fossa cyst at the fourth ventricle [hp:0000933]
Posterior fossa cyst at the fourth ventricle

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.
Impaired distal proprioception [hp:0006858]

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.

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.

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.
Abnormality of periauricular region [hp:0000383]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Increased intraocular pressure [hp:0007906]

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.

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.

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.
Obsessive-compulsive behavior [hp:0000722]

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.
Abnormality of male internal genitalia [hp:0000022]

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.
Stippled chondral calcification [hp:0002764]

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.

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.

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.

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.
Retinitis pigmentosa inversa [hp:0008035]

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.

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.
Flat distal femoral epiphysis [hp:0006398]

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.

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.

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.
Recurrent Haemophilus influenzae infections [hp:0005376]
Recurrent Haemophilus influenzae infections

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.

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.

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.

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.
Long-segment aganglionic megacolon [hp:0011285]

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.

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.

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.
Hypertrophic cardiomyopathy [hp:0001639]

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.

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.
Increased urinary thiosulfate [hp:0011943]

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.

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.
Microvesicular hepatic steatosis [hp:0001414]

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.
Palpebral fissure narrowing on adduction [hp:0000661]
Palpebral fissure narrowing on adduction

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.

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.

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.

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.

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.

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.

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.
Multiple epiphyseal dysplasia [hp:0002654]

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.
Contractures involving the joints of the feet [hp:0008366]
Contractures involving the joints of the feet

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.

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.

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.

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.

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.
Paroxysmal bursts of laughter [hp:0000749]

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.
Dagger-shaped pulp calcifications [hp:0006302]

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.

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.
Crossed fused renal ectopia [hp:0004736]

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.
Intermittent episodes of respiratory insufficiency due to muscle weakness [hp:0004889]
Intermittent episodes of respiratory insufficiency due to muscle weakness

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.

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.

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.
Type I transferrin isoform profile [hp:0003642]

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.
Severe expressive language delay [hp:0006863]

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.

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.

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.

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.

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.
Elevated 7-dehydrocholesterol [hp:0010569]

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.

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.
Cone-shaped epiphyses of phalanges 2 to 5 [hp:0006035]
Cone-shaped epiphyses of phalanges 2 to 5

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.

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.

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.
Partial duplication of the distal phalanx of the 3rd finger [hp:0009968]
Partial duplication of the distal phalanx of the 3rd finger

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.
Neonatal alloimmune thrombocytopenia [hp:0004809]

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.

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.
Olivopontocerebellar atrophy [hp:0002542]

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.
Absent anterior eye chamber [hp:0008037]

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.
Spondyloepiphyseal dysplasia [hp:0002655]

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.

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.

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.

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.

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.

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.
Abnormality of the vertebral column [hp:0000925]

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.

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.

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.
Bronchiolitis obliterans organizing pneumonia [hp:0011945]
Bronchiolitis obliterans organizing pneumonia

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.

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.
Abnormality of the myocardium [hp:0001637]

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.

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.

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.

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.
Hyperkeratosis lenticularis perstans [hp:0007570]

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.

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.
Decreased corneal thickness [hp:0100689]

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.
Aplasia/Hypoplasia of the eyebrow [hp:0100840]

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.

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.

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.

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.

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.

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.

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.
Abnormality of the skeletal system [hp:0000924]

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.

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.

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.

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.

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.

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.
Respiratory failure requiring assisted ventilation [hp:0004887]
Respiratory failure requiring assisted ventilation

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.

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.

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.

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.

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.
Pulmonary venoocclusive disease [hp:0006518]

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.

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.
Partial cellular immunodeficiency [hp:0005375]

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.

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.
Spondylometaphyseal dysplasia [hp:0002657]

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.

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.

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.

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.

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.

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.

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.

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.

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.
Congenital laryngeal stridor [hp:0004886]

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.

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.
Deep longitudinal plantar crease [hp:0004681]

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.
Limited pronation/supination of forearm [hp:0006394]

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.

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.

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.

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.

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.

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.

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.
Radial deviation of the 4th finger [hp:0009279]

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.

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.

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.
Fusion of midphalangeal joints [hp:0006187]

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.

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.
Functional abnormality of male internal genitalia [hp:0000025]
Functional abnormality of male internal genitalia

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.
Congenital hemolytic anemia [hp:0004804]

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.

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.

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.

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.

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.

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.

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.

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.

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.
Episodic respiratory distress [hp:0004885]

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.
Sternal punctate calcifications [hp:0006637]

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.
Posterior Y-sutural cataract [hp:0008031]

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.

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.

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.

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.

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.

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.

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.

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.
Abnormality of the mitral valve [hp:0001633]

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.

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.

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.

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.

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.

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.

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.

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.

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.
Impaired ability to form peer relationships [hp:0000728]
Impaired ability to form peer relationships

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.
Increased susceptibility to fractures [hp:0002659]

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.

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.

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.

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.
Congenital fibrosis of extraocular muscles [hp:0001491]
Congenital fibrosis of extraocular muscles

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.

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.

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.

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.
Tubulointerstitial nephritis [hp:0001970]

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.

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.

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.
Enlarged proximal interphalangeal joints [hp:0006185]
Enlarged proximal interphalangeal joints

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.

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.
Weakness of long finger extensor muscles [hp:0009077]
Weakness of long finger extensor muscles

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.

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.

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.

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.

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.
Transient erythroblastopenia [hp:0005510]

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.

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.

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.

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.
Foam cells in visceral organs and CNS [hp:0003640]

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.

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.

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.

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.
Lateral displacement of patellae [hp:0006397]

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.
Absent ossification of calvaria [hp:0005623]

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.

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.
Hypomineralization of enamel [hp:0006285]

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.

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.
Decreased serum ceruloplasmin [hp:0010837]

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.
Rhegmatogenous retinal detachment [hp:0012230]

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.
First dorsal interossei muscle weakness [hp:0003392]

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.
Elevated maternal serum alpha-fetoprotein [hp:0005984]
Elevated maternal serum alpha-fetoprotein

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.
Chromosomal breakage induced by crosslinking agents [hp:0003221]
Chromosomal breakage induced by crosslinking agents

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.
First dorsal interossei muscle atrophy [hp:0003426]

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.
Pulmonary arteriovenous fistulas [hp:0004952]

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.
Overgrowth of external genitalia [hp:0003247]

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.
Reduction of neutrophil motility [hp:0005400]

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.

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.

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.

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.

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.
Long chain 3 hydroxyacyl coA dehydrogenase deficiency [hp:0100950]
Long chain 3 hydroxyacyl coA dehydrogenase deficiency

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.

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.

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.

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.

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.
Parkinsonism with favorable response to dopaminergic medication [hp:0002548]
Parkinsonism with favorable response to dopaminergic medication

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.

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.

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.
Recurrent aphthous stomatitis [hp:0011107]

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.
Anxiety (with pheochromocytoma) [hp:0000740]

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.
Abnormality of the antitragus [hp:0009896]

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.
Distal lower limb amyotrophy [hp:0008944]

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.
Yellow-brown discoloration of the teeth [hp:0006286]

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.
Mildly elevated creatine phosphokinase [hp:0008180]

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.

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.

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.
Deficit in phonologic short-term memory [hp:0002549]

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.
Exudative retinal detachment [hp:0012231]

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.

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.

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.

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.

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.
Gonadal tissue inappropriate for external genitalia or chromosomal sex [hp:0003248]
Gonadal tissue inappropriate for external genitalia or chromosomal sex

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.
Enlarged fossa interpeduncularis [hp:0100951]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Abnormality of the hip joint [hp:0001384]

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.

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.
Loss of ability to walk in early childhood [hp:0008945]
Loss of ability to walk in early childhood

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.

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.

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.

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.

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.

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.

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.

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.

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.
Aplasia/hypoplasia of the extremities [hp:0009815]

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.

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.
Facial palsy secondary to cranial hyperostosis [hp:0007285]
Facial palsy secondary to cranial hyperostosis

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.

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.

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.

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.
Abnormal cervical curvature [hp:0005905]

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.

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.

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.
Chronic monilial nail infection [hp:0008396]

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.

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.
Anesthetic-induced rhabdomylosis [hp:0011439]

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.
Increased cellular sensitivity to UV light [hp:0003224]
Increased cellular sensitivity to UV light

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.

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.

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.

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.
Hypoplasia of the calcaneus [hp:0012789]

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.

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.

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.
Recurrent candida infections [hp:0005401]

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.

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.
Thoracolumbar kyphoscoliosis [hp:0003423]

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.

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.
Periventricular leukomalacia [hp:0006970]

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.
Generalized arterial tortuosity [hp:0004955]

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.
Progressive proximal muscle weakness [hp:0009073]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Increased density of long bones [hp:0006392]

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.

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.

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.
Infantile muscular hypotonia [hp:0008947]

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.

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.

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.
Photosensitive tonic-clonic seizures [hp:0007207]

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.

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.
Premature delivery because of cervical insufficiency or membrane fragility [hp:0005267]
Premature delivery because of cervical insufficiency or membrane fragility

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.
Vertebral segmentation defect [hp:0003422]

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.

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.
Prolonged partial thromboplastin time [hp:0003645]

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.

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.

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.
Congenital muscular torticollis [hp:0005988]

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.
Aplasia/Hypoplasia of the hallux [hp:0008362]

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.
Underdeveloped supraorbital ridges [hp:0009891]

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.
Social and occupational deterioration [hp:0007086]

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.

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.

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.
Involuntary jerking movements [hp:0007087]

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.
Hypoplastic fifth fingernail [hp:0008398]

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.

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.
Aplasia of the parotid gland [hp:0009740]

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.
Aplasia/Hypoplasia of the tarsal bones [hp:0008363]

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.

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.

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.

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.

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.

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.

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.

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.

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.
Generalized lymphadenopathy [hp:0008940]

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.

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.
Irregular distal femoral epiphysis [hp:0006407]

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.

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.

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.
Pigmented paravenous chorioretinal atrophy [hp:0007903]
Pigmented paravenous chorioretinal atrophy

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.

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.
Impaired renal uric acid clearance [hp:0004732]

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.

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.
Generalized hypotonia due to defect at the neuromuscular junction [hp:0003397]
Generalized hypotonia due to defect at the neuromuscular junction

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.
Concentric hypertrophic cardiomyopathy [hp:0005157]

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.

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.
Pseudoepiphyses of the 2nd finger [hp:0009495]

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.

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.

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.
Patchy demyelination of subcortical white matter [hp:0002545]
Patchy demyelination of subcortical white matter

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.
Absent in utero ossification of vertebral bodies [hp:0008435]
Absent in utero ossification of vertebral bodies

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.

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.

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.

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.
Abnormality of calcium-phosphate metabolism [hp:0100530]
Abnormality of calcium-phosphate metabolism

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.

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.
Right ventricular cardiomyopathy [hp:0011663]

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.

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.

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.
Electron transfer flavoprotein-ubiquinone oxidoreductase defect [hp:0003647]
Electron transfer flavoprotein-ubiquinone oxidoreductase defect

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.

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.

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.

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.

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.

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.
Precocious puberty in males [hp:0008185]

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.

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.
External genital hypoplasia [hp:0003241]

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.

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.

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.
Spondyloepimetaphyseal dysplasia [hp:0002651]

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.

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.
Facial-lingual fasciculations [hp:0007089]

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.

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.
Diffuse white matter abnormalities [hp:0007204]

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.

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.
Inflammatory abnormality of the eye [hp:0100533]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Abnormality of chromosome stability [hp:0003220]

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.
Iridescent posterior subcapsular cataract [hp:0007889]
Iridescent posterior subcapsular cataract

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.

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.
High nonceruloplasmin-bound serum copper [hp:0010838]
High nonceruloplasmin-bound serum copper

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.
Peripheral visual field loss [hp:0007994]

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.

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.

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.
Absence of secondary sex characteristics [hp:0008187]
Absence of secondary sex characteristics

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.

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.
Abnormality of the calcaneus [hp:0008364]

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.

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.

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.

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.
Apneic episodes precipitated by illness, fatigue, stress [hp:0002872]
Apneic episodes precipitated by illness, fatigue, stress

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.

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.

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.
Abnormality of the salivary glands [hp:0010286]

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.

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.

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.

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.
Very long chain fatty acid accumulation [hp:0008167]

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.
Cervical spinal canal stenosis [hp:0008445]

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.

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.

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.

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.

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.
Nevus flammeus of the forehead [hp:0007413]

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.

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.
Gastrointestinal stroma tumor [hp:0100723]

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.

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.

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.
Transitional cell carcinoma of the bladder [hp:0006740]
Transitional cell carcinoma of the bladder

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.
Widely patent sagittal suture [hp:0005476]

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.
High intestinal obstruction [hp:0005250]

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.
Joint contracture of the 5th finger [hp:0009183]

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.

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.
Fingerprint intracellular accumulation of autofluorescent lipopigment storage material [hp:0003208]
Fingerprint intracellular accumulation of autofluorescent lipopigment storage material

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.

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.

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.
Crystalline corneal dystrophy [hp:0007760]

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.

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.
Aplasia/Hypoplasia of the fibula [hp:0006492]

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.

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.
Decreased beta-galactosidase activity [hp:0008166]

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.
Neonatal wrinkled skin of hands and feet [hp:0007414]
Neonatal wrinkled skin of hands and feet

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.

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.

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.

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.

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.

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.
Excessive daytime sleepiness [hp:0002189]

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.
Linear arrays of macular hyperkeratoses in flexural areas [hp:0007490]
Linear arrays of macular hyperkeratoses in flexural areas

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.

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.
Olivopontocerebellar hypoplasia [hp:0006955]

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.

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.

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.

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.

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.
Patchy palmoplantar keratoderma [hp:0005588]

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.
Pancreatic islet-cell hyperplasia [hp:0004510]

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.

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.
Reduced circulating T-helper cells [hp:0008165]

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.
EEG with photoparoxysmal response [hp:0010852]

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.
Abnormality of the tibial metaphysis [hp:0006491]

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.

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.

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.
Discrete 2 to 5-mm hyper- and hypopigmented macules [hp:0007494]
Discrete 2 to 5-mm hyper- and hypopigmented macules

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.

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.
Mediastinal lymphadenopathy [hp:0100721]

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.

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.

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.

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.
Hypoplastic-absent sebaceous glands [hp:0007411]

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.

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.

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.

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.
Episodes of ventricular tachycardia [hp:0005141]

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.
Contracture of the proximal interphalangeal joint of the 5th finger [hp:0009185]
Contracture of the proximal interphalangeal joint of the 5th finger

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.

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.
Hyperactive patellar reflex [hp:0007083]

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.
Short distal phalanx of the 4th finger [hp:0009290]

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.

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.
Decreased activity of NADPH oxidase [hp:0003206]

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.

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.
Posterior wedging of vertebral bodies [hp:0008444]

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.

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.
Partially duplicated kidney [hp:0008738]

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.

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.
Progressive peripheral neuropathy [hp:0007133]

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.

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.

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.
Hypoplasia of the ear cartilage [hp:0100720]

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.
Progressive sclerosis of skull base [hp:0005477]

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.

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.

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.

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.
Abnormality of the vitreous humor [hp:0004327]

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.
Curvilinear intracellular accumulation of autofluorescent lipopigment storage material [hp:0003205]
Curvilinear intracellular accumulation of autofluorescent lipopigment storage material

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.

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.

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.
Decreased circulating cortisol level [hp:0008163]

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.

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.

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.

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.

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.
Complete duplication of distal phalanx of the thumb [hp:0009606]
Complete duplication of distal phalanx of the thumb

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.

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.
Bilateral conductive hearing impairment [hp:0008513]

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.

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.
Abnormality of the menstrual cycle [hp:0000140]

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.
Interstitial pulmonary disease [hp:0006530]

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.
Aplasia/Hypoplasia of the patella [hp:0006498]

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.

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.

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.

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.

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.

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.
Abnormal auditory evoked potentials [hp:0006958]

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.

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.

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.
Decreased retinal pigmentation with dispersion [hp:0007659]
Decreased retinal pigmentation with dispersion

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.

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.
Rectilinear intracellular accumulation of autofluorescent lipopigment storage material [hp:0003226]
Rectilinear intracellular accumulation of autofluorescent lipopigment storage material

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.

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.

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.

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.
First degree atrioventricular block [hp:0011705]

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.
Abnormal sternal ossification [hp:0011863]

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.

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.
Pyramidal skinfold extending from the base to the top of the nails [hp:0009758]
Pyramidal skinfold extending from the base to the top of the nails

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.

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.

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.

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.

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.

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.

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.

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.

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.
Increased upper to lower segment ratio [hp:0012774]

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.

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.

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.
Negative nitroblue tetrazolium (NBT) reduction test [hp:0003203]
Negative nitroblue tetrazolium (NBT) reduction test

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.

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.
Reduced phenylalanine hydroxylase activity [hp:0005982]
Reduced phenylalanine hydroxylase activity

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.

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.

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.

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.

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.
Intrauterine growth retardation [hp:0001511]

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.

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.
Complete duplication of proximal phalanx of the thumb [hp:0009608]
Complete duplication of proximal phalanx of the thumb

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.
Elevated plasma pyrophosphate [hp:0011864]

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.
Conjunctival telangiectasia [hp:0000524]

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.

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.

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.

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.
Reduced factor VII activity [hp:0008169]

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.
Dilation of lateral ventricles [hp:0006956]

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.

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.

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.
Recurrent loss of toenails and fingernails [hp:0008390]
Recurrent loss of toenails and fingernails

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.
Decreased calvarial ossification [hp:0005474]

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.
Recurrent cutaneous abscess formation [hp:0100838]

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.

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.

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.
Bowing of limbs due to multiple fractures [hp:0003023]
Bowing of limbs due to multiple fractures

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.

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.

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.

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.
Degeneration of the lateral corticospinal tracts [hp:0002314]
Degeneration of the lateral corticospinal tracts

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.
Proximal upper limb amyotrophy [hp:0008948]

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.

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.
C1-C2 vertebral abnormality [hp:0008440]

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.

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.

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.

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.

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.

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.
Aplasia/Hypoplasia of the ulna [hp:0006495]

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.

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.

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.
Large hyperpigmented retinal spots [hp:0007658]

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.

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.

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.
Fusion of middle ear ossicles [hp:0005473]

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.

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.
Fava bean-induced hemolytic anemia [hp:0004814]

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.

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.

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.
Central retinal vessel vascular tortuosity [hp:0007768]
Central retinal vessel vascular tortuosity

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.

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.

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.

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.
Eversion of lateral third of lower eyelids [hp:0007655]
Eversion of lateral third of lower eyelids

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.
Aplasia/Hypoplasia of the iris [hp:0008053]

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.

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.
Hypodysplasia of the corpus callosum [hp:0006849]

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.

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.

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.
Abnormality of thumb phalanx [hp:0009602]

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.

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.
Abnormal diaphysis morphology [hp:0000940]

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.

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.

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.

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.

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.
Aplasia/Hypoplasia of the sacrum [hp:0008517]

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.

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.

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.

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.

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.
Duplication of renal pelvis [hp:0005580]

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.

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.

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.

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.
Post-transfusion thrombocytopenia [hp:0004813]

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.
Benign neoplasm of the central nervous system [hp:0100835]
Benign neoplasm of the central nervous system

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.

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.

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.

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.

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.

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.

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.
Hypersegmentation of proximal phalanx of third finger [hp:0011929]
Hypersegmentation of proximal phalanx of third finger

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.

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.

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.

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.
Aplasia/Hypoplasia of the thumb [hp:0009601]

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.

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.

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.

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.

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.
Abnormality of the vertebral spinous processes [hp:0008516]
Abnormality of the vertebral spinous processes

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.
Autonomic erectile dysfunction [hp:0008652]

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.
Diffuse swelling of cerebral white matter [hp:0007341]
Diffuse swelling of cerebral white matter

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.
Recurrent staphylococcal infections [hp:0007499]

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.

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.

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.

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.

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.

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.
Tubular basement membrane disintegration [hp:0005583]
Tubular basement membrane disintegration

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.
Inflammation of the large intestine [hp:0002037]

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.

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.
Abnormality of the nervous system [hp:0000707]

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.

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.

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.

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.

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.
Elevated levels of phytanic acid [hp:0010571]

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.

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.

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.
Postlingual sensorineural hearing impairment [hp:0008596]
Postlingual sensorineural hearing impairment

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.

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.
Absent microvilli on the surface of peripheral blood lymphocytes [hp:0002971]
Absent microvilli on the surface of peripheral blood lymphocytes

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.
Incomplete partition of the cochlea type II [hp:0000376]
Incomplete partition of the cochlea type II

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.
Gastrointestinal hemorrhage [hp:0002239]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Increased serum bile acid concentration during pregnancy [hp:0200150]
Increased serum bile acid concentration during pregnancy

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.
Absent neutrophil specific granules [hp:0012551]

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.
Abnormality of the palpebral fissures [hp:0008050]

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.

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.
Abnormal mitochondrial shape [hp:0012087]

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.

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.

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.

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.

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.

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.

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.

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.
Triangular shaped middle phalanx of the 3rd finger [hp:0009436]
Triangular shaped middle phalanx of the 3rd finger

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.
Neoplasm of the small intestine [hp:0100833]

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.
Female external genitalia in individual with 46,XY karyotype [hp:0008730]
Female external genitalia in individual with 46,XY karyotype

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.

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.

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.

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.

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.

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.
Multiple cafe-au-lait spots [hp:0007565]

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.
Proportionate short stature [hp:0003508]

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.
Elevated alkaline phosphatase of bone origin [hp:0010639]
Elevated alkaline phosphatase of bone origin

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.

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.

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.

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.
Abnormality of the metaphyses [hp:0000944]

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.

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.
Recurrent bronchopulmonary infections [hp:0006538]

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.

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.

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.
Congenital hypoplastic anemia [hp:0004810]

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.

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.

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.

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.

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.
Shortening of all middle phalanges of the fingers [hp:0006110]
Shortening of all middle phalanges of the fingers

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.

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.
Disproportionate short-limb short stature [hp:0008873]
Disproportionate short-limb short stature

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.

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.
Atrophy/Degeneration involving the spinal cord [hp:0007344]
Atrophy/Degeneration involving the spinal cord

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.

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.

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.
Discoid lupus erythematosus [hp:0007417]

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.
Abnormality of the middle ear [hp:0000370]

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.
Bracket epiphysis of the middle phalanx of the 5th finger [hp:0009204]
Bracket epiphysis of the middle phalanx of the 5th finger

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.

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.

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.
EEG with centrotemporal focal spike waves [hp:0012557]
EEG with centrotemporal focal spike waves

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.

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.

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.

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.

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.
Aplasia of metacarpal bones [hp:0010048]

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.
Decreased activity of mitochondrial ATP synthase complex [hp:0011925]
Decreased activity of mitochondrial ATP synthase complex

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.
Bronchial cartilage hypoplasia [hp:0006539]

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.
Abnormal vertebral segmentation and fusion [hp:0005640]
Abnormal vertebral segmentation and fusion

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.

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.

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.

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.
Macrovesicular hepatic steatosis [hp:0001403]

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.
Reduced delayed hypersensitivity [hp:0002972]

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.
Prematurely aged appearance [hp:0007495]

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.

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.

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.
Acute demyelinating polyneuropathy [hp:0007131]

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.

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.

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.

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.

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.

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.

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.

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.
Profuse pigmented skin lesions [hp:0005587]

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.
Decreased activity of mitochondrial complex III [hp:0011924]
Decreased activity of mitochondrial complex III

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.

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.

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.

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.

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.

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.

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.

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.
Abnormality of the auditory canal [hp:0000372]

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.

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.

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.
Flexion contracture of thumb [hp:0009600]

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.

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.

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.
Intellectual disability, profound [hp:0002187]

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.
Progressive ophthalmoplegia [hp:0007650]

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.
Triangular shaped middle phalanx of the 5th finger [hp:0009182]
Triangular shaped middle phalanx of the 5th finger

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.

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.

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.

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.

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.

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.

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.
Decreased activity of mitochondrial complex I [hp:0011923]
Decreased activity of mitochondrial complex I

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.
Hyperpigmentation in sun-exposed areas [hp:0005586]

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.
Susceptibility to chickenpox [hp:0005360]

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.
Cortical thickening of long bone diaphyses [hp:0005791]
Cortical thickening of long bone diaphyses

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.

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.

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.

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.
Feeding difficulties in infancy [hp:0008872]

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.

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.

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.

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.

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.

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.
Decreased pyruvate carboxylase activity [hp:0003209]

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.

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.
Generalized seborrheic dermatitis [hp:0007569]

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.

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.

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.

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.

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.

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.
Neonatal respiratory distress [hp:0002643]

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.

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.

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.

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.
Delayed skeletal maturation [hp:0002750]

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.

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.

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.
Elongated superior cerebellar peduncle [hp:0011933]

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.

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.
Progressive visual field defects [hp:0007987]

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.

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.

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.
Circulating immune complexes [hp:0012224]

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.
Reduced activity of N-acetylglucosaminyltransferase II [hp:0003655]
Reduced activity of N-acetylglucosaminyltransferase II

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.
Almond-shaped palpebral fissure [hp:0007874]

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.

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.
Radial metaphyseal irregularity [hp:0004019]

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.

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.
Proximal radio-ulnar synostosis [hp:0005037]

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.

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.

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.
Hypoplasia of the pyramidal tract [hp:0007348]

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.

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.
Multiple small medullary renal cysts [hp:0008659]

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.
Abnormality of pelvic girdle bone morphology [hp:0002644]
Abnormality of pelvic girdle bone morphology

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.
Distal widening of metacarpals [hp:0006048]

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.
Hepatic abscesses due to immunodeficiency [hp:0001400]
Hepatic abscesses due to immunodeficiency

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.

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.

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.
Aplasia/Hypoplasia involving the central nervous system [hp:0002977]
Aplasia/Hypoplasia involving the central nervous system

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.

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.
Macrodontia of permanent maxillary central incisor [hp:0000675]
Macrodontia of permanent maxillary central incisor

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.
Partial humoral immunodeficiency [hp:0005363]

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.
Decreased beta-glucocerebrosidase protein and activity [hp:0003656]
Decreased beta-glucocerebrosidase protein and activity

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.

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.

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.

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.

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.
Abnormality of the cardiovascular system [hp:0001626]
Abnormality of the cardiovascular system

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.

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.
Abnormality of the intestine [hp:0002242]

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.
Abnormally prominent line of Schwalbe [hp:0007873]

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.

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.

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.
Decreased movement range in interphalangeal joints [hp:0006203]
Decreased movement range in interphalangeal joints

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.
Impaired social interactions [hp:0000735]

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.
Prominent supraorbital arches in adult [hp:0004676]

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.
Hyperextensible hand joints [hp:0005639]

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.
Decreased number of large peripheral myelinated nerve fibers [hp:0003387]
Decreased number of large peripheral myelinated nerve fibers

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.

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.

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.

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.

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.

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.

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.
Normocytic hypoplastic anemia [hp:0004819]

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.

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.
Intrahepatic biliary dysgenesis [hp:0001401]

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.

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.

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.

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.

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.
Abnormality of creatine metabolism [hp:0012113]

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.
Single median maxillary incisor [hp:0006315]

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.

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.
Abnormality of cardiac morphology [hp:0001627]

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.
Decreased facial expression [hp:0004673]

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.

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.
Thimble-shaped middle phalanges of hand [hp:0006193]

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.
Episodic generalized hypotonia [hp:0006852]

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.

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.
Shortening of all phalanges of the toes [hp:0005035]

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.

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.

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.
Hypoplastic distal radial epiphyses [hp:0006386]

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.

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.

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.
Retinal arteriolar occlusion [hp:0007985]

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.

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.

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.

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.
Abnormality of the clavicle [hp:0000889]

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.

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.

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.
Arteriovenous fistulas of celiac and mesenteric vessels [hp:0002642]
Arteriovenous fistulas of celiac and mesenteric vessels

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.

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.

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.
Expanded phalanges with widened medullary cavities [hp:0006112]
Expanded phalanges with widened medullary cavities

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.

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.
Subcortical white matter calcifications [hp:0007346]

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.

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.
Reduced dihydropyrimidine dehydrogenase activity [hp:0003654]
Reduced dihydropyrimidine dehydrogenase activity

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.

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.

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.

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.

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.
Abnormality of the small intestine [hp:0002244]

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.

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.

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.
Cerebellar hemisphere hypoplasia [hp:0100307]

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.
Symmetric spinal nerve root neurofibromas [hp:0006851]
Symmetric spinal nerve root neurofibromas

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.

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.
Abnormality of dental color [hp:0011073]

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.

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.
Hypermobility of distal interphalangeal joints [hp:0006201]
Hypermobility of distal interphalangeal joints

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.

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.
Reduced amplitude of b-wave (ERG) [hp:0007984]

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.

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.
Impaired thermal sensitivity [hp:0006901]

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.
Wide distal femoral metaphysis [hp:0006387]

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.

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.

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.
Reduced lymphocyte surface expression of CD43 (sialophorin) [hp:0001983]
Reduced lymphocyte surface expression of CD43 (sialophorin)

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.
Incomplete male pseudohermaphroditism [hp:0008656]

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.

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.

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.
Paucity of anterior horn motor neurons [hp:0007277]

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.
Enlarged flash visual evoked potentials [hp:0008045]

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.

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.
Hypoplasia of the lesser trochanter [hp:0008801]

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.

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.
Stenosis of the medullary cavity of the long bones [hp:0100254]
Stenosis of the medullary cavity of the long bones

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.

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.
Proximal tapering of metacarpals [hp:0006119]

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.
Congenital intracerebral calcification [hp:0006906]

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.

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.

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.

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.

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.
Absent sternal ossification [hp:0006628]

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.

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.

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.
Abnormality of radial metaphyses [hp:0004015]

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.

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.
Hypoplasia of the ventral pons [hp:0006850]

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.

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.

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.

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.

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.
Recurrent streptococcus pneumoniae infections [hp:0005366]
Recurrent streptococcus pneumoniae infections

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.
Aplasia/Hypoplasia of the fallopian tube [hp:0008655]
Aplasia/Hypoplasia of the fallopian tube

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.

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.
Paroxysmal nocturnal hemoglobinuria [hp:0004818]

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.

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.

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.

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.
Abnormality of the medullary cavity of the long bones [hp:0100253]
Abnormality of the medullary cavity of the long bones

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.
Osteomyelitis due to immunodeficiency [hp:0002755]

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.
Abnormality of the retinal vasculature [hp:0008046]

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.
Hypoplasia of the femoral head [hp:0008802]

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.

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.

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.
Shortening of all distal phalanges of the fingers [hp:0006118]
Shortening of all distal phalanges of the fingers

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.

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.
Abnormality of calvarial morphology [hp:0002648]

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.

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.

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.

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.

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.

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.

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.

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.

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.
Cutaneous finger syndactyly [hp:0010554]

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.

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.

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.
Abnormality of the metacarpal bones [hp:0001163]

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.
Telangiectases in sun-exposed and nonexposed skin [hp:0007561]
Telangiectases in sun-exposed and nonexposed skin

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.

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.

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.

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.

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.

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.

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.

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.

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.
Abnormality of the dorsal column of the spinal cord [hp:0011397]
Abnormality of the dorsal column of the spinal cord

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.
Calcaneal epiphyseal stippling [hp:0004695]

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.

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.

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.
Late-onset spinocerebellar degeneration [hp:0006904]

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.

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.

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.

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.

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.

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.
Multiple long-bone exostoses [hp:0005039]

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.

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.

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.
Muscle fiber cytoplasmatic inclusion bodies [hp:0100303]
Muscle fiber cytoplasmatic inclusion bodies

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.

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.

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.

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.

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.

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.
Dysplasia of the femoral head [hp:0010575]

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.

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.

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.

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.
Retinal arteriolar constriction [hp:0008043]

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.

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.
Progressive bowing of long bones [hp:0006383]

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.

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.

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.
Decreased serum complement factor H [hp:0005369]

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.

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.

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.

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.
Stress/infection-induced lactic acidosis [hp:0004897]
Stress/infection-induced lactic acidosis

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.
Progressive distal muscle weakness [hp:0009063]

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.
Progressive psychomotor deterioration [hp:0007272]

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.

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.
Prolonged miniature endplate currents [hp:0003436]

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.

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.

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.

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.

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.

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.
Extraadrenal pheochromocytoma [hp:0006737]

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.

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.
Aplasia/Hypoplasia of the tongue [hp:0010295]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Pectoral muscle hypoplasia/aplasia [hp:0005258]

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.

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.

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.

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.
Distal upper limb muscle weakness [hp:0008959]

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.

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.

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.

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.

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.

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.

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.
Recurrent bacterial meningitis [hp:0007274]

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.

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.

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.

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.
Pulmonary arterial medial hypertrophy [hp:0004964]

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.

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.

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.
Decreased skull ossification [hp:0004331]

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.

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.
Decreased resting energy expenditure [hp:0012340]

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.
Abnormality of femoral epiphysis [hp:0006499]

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.

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.
Abnormal facility in opposing the shoulders [hp:0005259]
Abnormal facility in opposing the shoulders

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.
Decreased number of peripheral myelinated nerve fibers [hp:0003380]
Decreased number of peripheral myelinated nerve fibers

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.

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.
EEG with spike-wave complexes (>3.5 Hz) [hp:0010849]

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.

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.

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.
Proximal lower limb amyotrophy [hp:0008956]

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.
Aplasia/Hypoplasia of the uvula [hp:0010293]

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.

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.
Medullary thyroid carcinoma [hp:0002865]

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.

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.

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.

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.

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.
Abnormality of the metatarsal bones [hp:0001832]

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.

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.

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.
Decreased methylmalonyl-CoA mutase activity [hp:0003210]
Decreased methylmalonyl-CoA mutase activity

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.
Elevated serum creatine phosphokinase [hp:0003236]

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.
Reduced pancreatic beta cells [hp:0006274]

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.

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.

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.
Thyroid follicular hyperplasia [hp:0008225]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Non-caseating epithelioid cell granulomatosis [hp:0012220]
Non-caseating epithelioid cell granulomatosis

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.

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.

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.

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.
Metaphyseal cupping of proximal phalanges [hp:0006208]
Metaphyseal cupping of proximal phalanges

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.

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.
Chronic tubulointerstitial nephritis [hp:0004743]

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.
Increased anterioposterior diameter of thorax [hp:0005253]
Increased anterioposterior diameter of thorax

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.

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.

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.

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.

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.

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.
Abnormality of the acetabulum [hp:0003170]

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.

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.

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.
Agenesis of corpus callosum [hp:0001274]

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.

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.

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.

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.
Abnormality of the toenails [hp:0008388]

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.

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.
Bidirectional ventricular ectopy [hp:0005147]

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.
Decreased motor nerve conduction velocity [hp:0003431]
Decreased motor nerve conduction velocity

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.

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.

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.
Gait instability, worse in the dark [hp:0006962]

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.
Abnormality of the renal collecting system [hp:0004742]
Abnormality of the renal collecting system

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.

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.

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.

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.
Unilateral chest hypoplasia [hp:0005254]

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.

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.

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.
Abnormality of the corpus callosum [hp:0001273]

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.

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.

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.
Progressive cervical vertebral spine fusion [hp:0008449]
Progressive cervical vertebral spine fusion

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.

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.

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.
Hypertension associated with pheochromocytoma [hp:0002640]
Hypertension associated with pheochromocytoma

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.

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.
Progressive distal muscular atrophy [hp:0008955]

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.
Aplasia of the pectoralis major muscle [hp:0009751]

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.

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.
Decreased amplitude of sensory action potentials [hp:0007078]
Decreased amplitude of sensory action potentials

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.

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.
Squamous cell carcinoma of the skin [hp:0006739]

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.
Concentric narrowing of visual fields [hp:0007981]

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.
Left ventricular septal hypertrophy [hp:0005144]

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.

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.

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.
Hyperkalemic metabolic acidosis [hp:0005976]

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.

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.

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.
Absence of pectoralis minor muscle [hp:0005255]

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.

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.
Hypersegmentation of proximal phalanx of second finger [hp:0006206]
Hypersegmentation of proximal phalanx of second finger

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.

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.

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.

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.
Recurrent cerebral hemorrhage [hp:0004968]

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.

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.
Granular osmiophilic deposits (GROD) in cells [hp:0003657]
Granular osmiophilic deposits (GROD) in cells

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.

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.

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.

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.

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.

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.

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.

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.
Aplasia/Hypoplasia of the nails [hp:0008386]

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.
Inflexible adherence to routines or rituals [hp:0000732]
Inflexible adherence to routines or rituals

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.

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.

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.

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.
Hypochloremic metabolic alkalosis [hp:0005977]

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.
Absent retinal pigment epithelium [hp:0007980]

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.

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.

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.
Mitochondrial malic enzyme reduced [hp:0003232]

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.

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.

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.

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.
Unilateral absence of pectoralis major muscle [hp:0005256]
Unilateral absence of pectoralis major muscle

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.

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.

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.

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.

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.
Elevated serum long-chain fatty acids [hp:0045016]

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.
Disproportionate tall stature [hp:0001519]

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.
Choroid plexus calcification [hp:0006960]

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.

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.

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.

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.
Peripheral pulmonary artery stenosis [hp:0004969]

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.
Pectoralis major hypoplasia [hp:0008953]

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.

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.

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.

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.

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.
Left anterior fascicular block [hp:0011711]

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.
Extrapyramidal muscular rigidity [hp:0007076]

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.

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.
Abnormal trabecular bone morphology [hp:0100671]

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.

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.
Hypoplastic coccygeal vertebrae [hp:0008447]

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.

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.

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.
T-wave inversion in the right precordial leads [hp:0003140]
T-wave inversion in the right precordial leads

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.
Abnormality of vision evoked potentials [hp:0000649]

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.

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.
Type 1 muscle fiber atrophy [hp:0011807]

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.
Calcification of falx cerebri [hp:0005462]

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.

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.
Calcific aortic valve stenosis [hp:0005173]

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.
Benign genitourinary tract neoplasm [hp:0006778]

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.

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.
Neuronal loss in central nervous system [hp:0002529]

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.
Narrow vertebral interpedicular distance [hp:0008450]
Narrow vertebral interpedicular distance

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.

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.
Intestinal pseudo-obstruction [hp:0004389]

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.

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.

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.
Posterior vertebral hypoplasia [hp:0008451]

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.
Left postterior fascicular block [hp:0005172]

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.

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.

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.

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.

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.

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.

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.
Conjunctival whitish salt-like deposits [hp:0007799]

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.
Diffuse reticular or finely nodular infiltrations [hp:0002207]
Diffuse reticular or finely nodular infiltrations

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.

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.
Widely patent fontanelles and sutures [hp:0004492]

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.

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.

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.

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.

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.

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.

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.
Granulovacuolar degeneration [hp:0002528]

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.
Morphological abnormality of the pyramidal tract [hp:0002062]
Morphological abnormality of the pyramidal tract

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.

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.
Post-angioplasty coronary artery restenosis [hp:0004761]
Post-angioplasty coronary artery restenosis

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.

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.

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.

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.

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.

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.

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.

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.

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.
Broad distal phalanx of the hallux [hp:0010077]

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.

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.

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.

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.
Childhood-onset truncal obesity [hp:0008915]

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.

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.

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.

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.

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.
Recurrent respiratory infections [hp:0002205]

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.

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.

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.

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.
Abnormal central microtubular pair morphology of respiratory motile cilia [hp:0012260]
Abnormal central microtubular pair morphology of respiratory motile cilia

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.
Cerebral white matter atrophy [hp:0012762]

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.

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.
Abnormality of the cerebrum [hp:0002060]

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.

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.

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.

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.

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.
Jerk-locked premyoclonus spikes [hp:0001351]

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.

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.

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.
Hypointensity of cerebral white matter on MRI [hp:0007103]
Hypointensity of cerebral white matter on MRI

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.

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.

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.
Demyelinating motor neuropathy [hp:0007220]

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.

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.

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.
Early ossification of capital femoral epiphyses [hp:0008797]
Early ossification of capital femoral epiphyses

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.

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.

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.

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.

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.

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.

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.

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.

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.
Ovarian papillary adenocarcinoma [hp:0006774]

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.

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.
Congenital hypertrophy of retinal pigment epithelium [hp:0007649]
Congenital hypertrophy of retinal pigment epithelium

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.

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.

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.

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.
Diffuse palmoplantar hyperkeratosis [hp:0007447]

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.

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.

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.
Intellectual disability, severe [hp:0010864]

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.

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.

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.

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.

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.

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.

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.

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.

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.
Oppositional defiant disorder [hp:0010865]

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.

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.

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.

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.
Abnormality of the nasal alae [hp:0000429]

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.

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.
Paroxysmal involuntary eye movements [hp:0007704]

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.

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.

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.
Renal juxtaglomerular cell hypertrophy/hyperplasia [hp:0000111]
Renal juxtaglomerular cell hypertrophy/hyperplasia

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.

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.

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.
Abnormality of the sacroiliac joint [hp:0100781]

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.

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.
Hyperkeratosis over edematous areas [hp:0007448]

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.
Short middle phalanx of the 2nd finger [hp:0009577]

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.

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.

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.

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.

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.

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.
Abnormality of dental morphology [hp:0006482]

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.

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.
Abnormal retinal pigmentation [hp:0007703]

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.
Craniofacial osteosclerosis [hp:0005464]

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.

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.

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.

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.
Abnormality of primary teeth [hp:0006481]

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.
Eye of the tiger anomaly of globus pallidus [hp:0002454]
Eye of the tiger anomaly of globus pallidus

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.
Degeneration of anterior horn cells [hp:0002398]

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.
Confetti-like hypopigmented macules [hp:0007449]

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.
Caudal interpedicular narrowing [hp:0008457]

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.

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.
Retinal vascular malformation [hp:0007797]

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.

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.
Complete heart block with narrow QRS complexes [hp:0005178]
Complete heart block with narrow QRS complexes

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.

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.
Abnormal ossification of hand bones [hp:0005921]

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.

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.

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.

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.
Pigmentary retinal deposits [hp:0007702]

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.

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.

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.

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.

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.

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.

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.

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.
Postaxial polysyndactyly of foot [hp:0005817]

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.

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.
Abnormality of the globus pallidus [hp:0002453]

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.

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.

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.
Progressive congenital scoliosis [hp:0008458]

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.
Pigmentary retinal degeneration [hp:0001146]

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.

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.
Bilateral triphalangeal thumbs [hp:0005707]

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.

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.

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.
Abnormal delayed hypersensitivity skin test [hp:0002963]
Abnormal delayed hypersensitivity skin test

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.

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.

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.

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.
Peripheral arteriovenous fistula [hp:0100784]

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.

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.

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.

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.
Pulmonary arteriovenous malformation [hp:0006548]

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.
Exaggerated cellular immune processes [hp:0005397]

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.

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.
Generalized tonic-clonic seizures [hp:0002069]

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.

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.
Bone marrow hypocellularity [hp:0005528]

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.

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.
Chronic rhinitis due to narrow nasal airway [hp:0004499]
Chronic rhinitis due to narrow nasal airway

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.

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.
Wide-cupped costochondral junctions [hp:0000910]

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.
Elevated serum acid phosphatase [hp:0003148]

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.

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.

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.
Bifid distal phalanx of the thumb [hp:0009611]

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.
Shortening of the talar neck [hp:0008117]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Cutaneous syndactyly between fingers 2 and 5 [hp:0005650]
Cutaneous syndactyly between fingers 2 and 5

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.

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.
Unilateral primary pulmonary dysgenesis [hp:0006549]

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.

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.

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.

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.

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.

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.

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.
2-3 toe cutaneous syndactyly [hp:0005709]

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.

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.
Generalized muscle hypertrophy [hp:0003720]

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.
Absence of Lutheran antigen on erythrocytes [hp:0010971]
Absence of Lutheran antigen on erythrocytes

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Peripheral pulmonary vessel aplasia [hp:0005316]

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.
Localized epidermolytic hyperkeratosis [hp:0007559]

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.
Triangular shaped middle phalanx of the 2nd finger [hp:0009575]
Triangular shaped middle phalanx of the 2nd finger

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.

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.

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.
Anemia of inadequate production [hp:0010972]

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.
Polycystic kidney dysplasia [hp:0000113]

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.

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.

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.
Hypoplasia of the frontal lobes [hp:0007333]

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.

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.

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.

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.

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.
Developmental stagnation at onset of seizures [hp:0006834]
Developmental stagnation at onset of seizures

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.

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.
Increased pulmonary vascular resistance [hp:0005317]

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.
Bilateral elbow dislocations [hp:0005021]

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.

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.

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.
Abnormal subcutaneous fat tissue distribution [hp:0007552]
Abnormal subcutaneous fat tissue distribution

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.

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.
EEG with polyspike wave complexes [hp:0002392]

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.

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.

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.

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.

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.
Hypoplasia of deltoid muscle [hp:0030241]

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.

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.

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.

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.

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.
Aplasia/Hypoplasia of the lens [hp:0008063]

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.
Macrocytic hemolytic disease [hp:0005524]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Congenital symmetrical palmoplantar keratosis [hp:0007553]
Congenital symmetrical palmoplantar keratosis

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.

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.
Hypoplastic male external genitalia [hp:0000050]

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.

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.

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.

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.
Triangular-shaped open mouth [hp:0200096]

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.

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.
Abnormality of immune system physiology [hp:0010978]

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.
Spontaneous hemolytic crises [hp:0005525]

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.
Pseudoepiphysis of the thumb [hp:0009693]

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.

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.

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.

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.
Congenital stationary night blindness [hp:0007642]

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.

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.

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.
Decreased adenosylcobalamin [hp:0003145]

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.

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.

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.
Agenesis of pulmonary vessels [hp:0005311]

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.

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.

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.
Abnormality of the genitourinary system [hp:0000119]

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.

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.

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.
Spinal arteriovenous malformation [hp:0002390]

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.
Recurrent opportunistic infections [hp:0005390]

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.

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.
Abnormality of the heart valves [hp:0001654]

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.

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.

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.

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.
Metatarsal diaphyseal endosteal sclerosis [hp:0008114]
Metatarsal diaphyseal endosteal sclerosis

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.
Complete heart block with broad RS complexes [hp:0005170]
Complete heart block with broad RS complexes

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.

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.

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.
Abnormal blistering of the skin [hp:0008066]

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.
Shoulder girdle muscle atrophy [hp:0003724]

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.
Abnormal anterior horn cell morphology [hp:0006802]

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.
Peripheral traction retinal detachment [hp:0007643]

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.
Aplasia/Hypoplasia of the skin [hp:0008065]

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.

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.

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.

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.

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.
Pulmonary aterial intimal fibrosis [hp:0005312]

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.

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.

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.
Respiratory insufficiency due to muscle weakness [hp:0002747]
Respiratory insufficiency due to muscle weakness

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Hyperactive deep tendon reflexes [hp:0006801]

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.

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.

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.

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.

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.

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.

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.
Peripheral nerve compression [hp:0003406]

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.

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.
Elevated mean arterial pressure [hp:0004972]

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.
Short metacarpals with rounded proximal ends [hp:0006161]
Short metacarpals with rounded proximal ends

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.
Exercise-induced lactic acidemia [hp:0004901]

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.

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.

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.
Decreased activity of mitochondrial complex IV [hp:0008347]
Decreased activity of mitochondrial complex IV

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.

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.

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.

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.
Bilateral cleft lip and palate [hp:0002744]

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.

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.
Impaired horizontal smooth pursuit [hp:0001151]

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.
Widened proximal tibial metaphyses [hp:0005028]

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.
Macrocytic dyserythropoietic anemia [hp:0005532]

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.
Soft tissue swelling of interphalangeal joints [hp:0006162]
Soft tissue swelling of interphalangeal joints

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.
Peripheral retinal pigmentation abnormalities [hp:0200099]
Peripheral retinal pigmentation abnormalities

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.
Refractory macrocytic anemia [hp:0004861]

Phenotype [hp:0005645] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Intervertebral disk calcification [hp:0005645]
Phenotype [hp:0003260] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002890] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008346] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased red cell sickling tendency [hp:0008346]
Phenotype [hp:0007338] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010481] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008812] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000271] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008056] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Aplasia/Hypoplasia affecting the eye [hp:0008056]
Phenotype [hp:0009830] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002745] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001882] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006163] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Enlarged metacarpophalangeal joints [hp:0006163]
Phenotype [hp:0003517] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Birth length greater than 97th percentile [hp:0003517]
Birth length greater than 97th percentile
Phenotype [hp:0000049] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008689] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001578] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001992] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001150] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011003] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003378] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Axonal degeneration/regeneration [hp:0003378]
Phenotype [hp:0000704] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001802] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005249] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Functional intestinal obstruction [hp:0005249]
Phenotype [hp:0000905] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Progressive clavicular acroosteolysis [hp:0000905]
Phenotype [hp:0004860] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Thiamine-responsive megaloblastic anemia [hp:0004860]
Thiamine-responsive megaloblastic anemia
Phenotype [hp:0005535] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011387] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Enlarged vestibular aqueduct [hp:0011387]
Phenotype [hp:0003729] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Enteroviral dermatomyositis syndrome [hp:0003729]
Phenotype [hp:0000871] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000270] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Delayed cranial suture closure [hp:0000270]
Phenotype [hp:0002742] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Recurrent Klebsiella infections [hp:0002742]
Phenotype [hp:0001657] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000048] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001995] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002810] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006160] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004902] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011002] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100669] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormal pigmentation of the oral mucosa [hp:0100669]
Abnormal pigmentation of the oral mucosa
Phenotype [hp:0003403] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
EMG: decremental response of compound muscle action potential to repetitive nerve stimulation [hp:0003403]
EMG: decremental response of compound muscle action potential to repetitive nerve stimulation
Phenotype [hp:0004975] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Erlenmeyer flask deformity of the femurs [hp:0004975]
Erlenmeyer flask deformity of the femurs
Phenotype [hp:0000705] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004660] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplasia of facial musculature [hp:0004660]
Phenotype [hp:0200008] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006990] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012313] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001658] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006615] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Absent in utero rib ossification [hp:0006615]
Phenotype [hp:0005534] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Transient myeloproliferative syndrome [hp:0005534]
Phenotype [hp:0000904] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001212] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001880] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000872] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008348] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Immunoglobulin IgG2 deficiency [hp:0008348]
Phenotype [hp:0009007] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000047] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007550] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypohidrosis or hyperhidrosis [hp:0007550]
Phenotype [hp:0001994] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000311] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002743] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Recurrent enteroviral infections [hp:0002743]
Phenotype [hp:0003376] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005307] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Postural hypotension with compensatory tachycardia [hp:0005307]
Postural hypotension with compensatory tachycardia
Phenotype [hp:0000877] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Insulin-resistant diabetes mellitus at puberty [hp:0000877]
Insulin-resistant diabetes mellitus at puberty
Phenotype [hp:0011304] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004661] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001804] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012047] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004866] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Impaired ADP-induced platelet aggregation [hp:0004866]
Impaired ADP-induced platelet aggregation
Phenotype [hp:0010546] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011381] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Aplasia of the semicircular canal [hp:0011381]
Phenotype [hp:0012312] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004905] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001437] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the musculature of the lower limbs [hp:0001437]
Abnormality of the musculature of the lower limbs
Phenotype [hp:0008569] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002812] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100861] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002740] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Recurrent E. coli infections [hp:0002740]
Phenotype [hp:0007335] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001885] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002893] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000046] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002677] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100391] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Short distal phalanx of the 5th toe [hp:0100391]
Phenotype [hp:0001155] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012191] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003264] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Deficiency of N-acetylglucosamine-1-phosphotransferase [hp:0003264]
Deficiency of N-acetylglucosamine-1-phosphotransferase
Phenotype [hp:0005306] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000878] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000902] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012046] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002967] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001803] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012311] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001438] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011382] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplasia of the semicircular canal [hp:0011382]
Phenotype [hp:0010545] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004904] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Maturity-onset diabetes of the young [hp:0004904]
Phenotype [hp:0100663] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007334] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Bilateral convulsive seizures [hp:0007334]
Phenotype [hp:0002741] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Recurrent Serratia marcescens infections [hp:0002741]
Recurrent Serratia marcescens infections
Phenotype [hp:0002894] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001886] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) [hp:0001886]
Osteomyelitis or necrosis, distal, due to sensory neuropathy (feet)
Phenotype [hp:0000045] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003409] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Distal sensory impairment of all modalities [hp:0003409]
Distal sensory impairment of all modalities
Phenotype [hp:0002678] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008568] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012548] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Fatty replacement of skeletal muscle [hp:0012548]
Phenotype [hp:0011302] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003261] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007862] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012194] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005309] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Peripheral vascular insufficiency [hp:0005309]
Phenotype [hp:0005025] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004864] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Refractory sideroblastic anemia [hp:0004864]
Phenotype [hp:0003514] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Deficiency or absence of cytochrome b(-245) [hp:0003514]
Deficiency or absence of cytochrome b(-245)
Phenotype [hp:0001806] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002814] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the lower limb [hp:0002814]
Phenotype [hp:0012049] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001508] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0045025] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000044] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypogonadotrophic hypogonadism [hp:0000044]
Phenotype [hp:0000640] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001883] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007928] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormal flash visual evoked potentials [hp:0007928]
Phenotype [hp:0001153] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000700] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009944] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Partial duplication of thumb phalanx [hp:0009944]
Phenotype [hp:0008232] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Elevated follicle stimulating hormone [hp:0008232]
Phenotype [hp:0009831] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002891] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000875] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008345] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplasia of the iris dilator muscle [hp:0008345]
Phenotype [hp:0000900] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003262] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Smooth muscle antibody positivity [hp:0003262]
Phenotype [hp:0004971] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Pulmonary artery hypoplasia [hp:0004971]
Phenotype [hp:0004664] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005026] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Mesomelic/rhizomelic limb shortening [hp:0005026]
Phenotype [hp:0005308] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Pulmonary artery vasoconstriction [hp:0005308]
Phenotype [hp:0008230] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Decreased testosterone in males [hp:0008230]
Phenotype [hp:0012462] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003375] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Narrow greater sacrosciatic notches [hp:0003375]
Phenotype [hp:0001805] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002813] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of limb bone morphology [hp:0002813]
Phenotype [hp:0004758] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Effort-induced polymorphic ventricular tachycardias [hp:0004758]
Effort-induced polymorphic ventricular tachycardias
Phenotype [hp:0012048] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0045026] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the mediastinum [hp:0045026]
Phenotype [hp:0100665] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100864] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002965] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001152] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010543] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0030034] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Diffuse glomerular basement membrane lamellation [hp:0030034]
Diffuse glomerular basement membrane lamellation
Phenotype [hp:0004906] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001884] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006619] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Anterior rib punctate calcifications [hp:0006619]
Phenotype [hp:0009832] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the distal phalanx of finger [hp:0009832]
Abnormality of the distal phalanx of finger
Phenotype [hp:0008231] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Macronodular adrenal hyperplasia [hp:0008231]
Phenotype [hp:0008344] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Elevated plasma branched chain amino acids [hp:0008344]
Elevated plasma branched chain amino acids
Phenotype [hp:0000876] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001217] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005819] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Short middle phalanx of finger [hp:0005819]
Phenotype [hp:0100660] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001571] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002673] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009942] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Duplication of thumb phalanx [hp:0009942]
Phenotype [hp:0002897] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007109] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009002] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Loss of truncal subcutaneous adipose tissue [hp:0009002]
Loss of truncal subcutaneous adipose tissue
Phenotype [hp:0100555] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004909] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypokalemic hypochloremic metabolic alkalosis [hp:0004909]
Hypokalemic hypochloremic metabolic alkalosis
Phenotype [hp:0001776] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Bilateral talipes equinovarus [hp:0001776]
Phenotype [hp:0005243] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Partial abdominal muscle agenesis [hp:0005243]
Phenotype [hp:0003621] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004757] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Paroxysmal atrial fibrillation [hp:0004757]
Phenotype [hp:0012469] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004552] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007712] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012258] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormal axonemal organization of respiratory motile cilia [hp:0012258]
Abnormal axonemal organization of respiratory motile cilia
Phenotype [hp:0003267] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Reduced orotidine 5-prime phosphate decarboxylase activity [hp:0003267]
Reduced orotidine 5-prime phosphate decarboxylase activity
Phenotype [hp:0002816] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010749] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005759] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006323] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Premature loss of primary teeth [hp:0006323]
Phenotype [hp:0000768] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002521] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009943] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Complete duplication of thumb phalanx [hp:0009943]
Phenotype [hp:0008233] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Decreased serum progesterone [hp:0008233]
Phenotype [hp:0002898] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007108] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Demyelinating peripheral neuropathy [hp:0007108]
Phenotype [hp:0010489] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004380] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011892] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002460] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004756] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001507] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005244] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Gastrointestinal infarctions [hp:0005244]
Phenotype [hp:0012468] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004381] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Supravalvular aortic stenosis [hp:0004381]
Phenotype [hp:0012259] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Absent inner and outer dynein arms [hp:0012259]
Phenotype [hp:0002815] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003268] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007713] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001218] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005758] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007063] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Aplasia of the inferior half of the cerebellar vermis [hp:0007063]
Aplasia of the inferior half of the cerebellar vermis
Phenotype [hp:0012195] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000769] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006266] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100280] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008341] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Distal renal tubular acidosis [hp:0008341]
Phenotype [hp:0002522] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011459] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000766] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008236] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Isosexual precocious puberty [hp:0008236]
Phenotype [hp:0007065] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Disorganization of the anterior cerebellar vermis [hp:0007065]
Disorganization of the anterior cerebellar vermis
Phenotype [hp:0002461] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Dense calcifications in the cerebellar dentate nucleus [hp:0002461]
Dense calcifications in the cerebellar dentate nucleus
Phenotype [hp:0000531] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002895] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Papillary thyroid carcinoma [hp:0002895]
Phenotype [hp:0100662] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009835] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Aplasia/Hypoplasia of the distal phalanges of the hand [hp:0009835]
Aplasia/Hypoplasia of the distal phalanges of the hand
Phenotype [hp:0004755] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Supraventricular tachycardia [hp:0004755]
Phenotype [hp:0010548] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007924] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Slow decrease in visual acuity [hp:0007924]
Phenotype [hp:0005241] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Total intestinal aganglionosis [hp:0005241]
Phenotype [hp:0003623] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007866] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001504] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012256] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003510] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012103] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the mitochondrion [hp:0012103]
Phenotype [hp:0009092] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Progressive alveolar ridge hypertropy [hp:0009092]
Phenotype [hp:0006267] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003370] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Flat capital femoral epiphysis [hp:0003370]
Phenotype [hp:0007064] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Progressive language deterioration [hp:0007064]
Phenotype [hp:0007793] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Macular retinal pigment epithelial mottling [hp:0007793]
Macular retinal pigment epithelial mottling
Phenotype [hp:0012198] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000879] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003265] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Neonatal hyperbilirubinemia [hp:0003265]
Phenotype [hp:0006999] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007710] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Peripheral vitreous opacities [hp:0007710]
Phenotype [hp:0002676] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007066] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Proximal limb muscle stiffness [hp:0007066]
Phenotype [hp:0007227] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002896] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100556] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010487] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009836] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Broad distal phalanx of finger [hp:0009836]
Phenotype [hp:0100661] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005242] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Extrahepatic biliary duct atresia [hp:0005242]
Phenotype [hp:0007925] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011813] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased cerebral lipofuscin [hp:0011813]
Phenotype [hp:0012257] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002817] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the upper limb [hp:0002817]
Phenotype [hp:0003371] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Enlargement of the proximal femoral epiphysis [hp:0003371]
Enlargement of the proximal femoral epiphysis
Phenotype [hp:0000767] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012197] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006268] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007792] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001772] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000421] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001575] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007440] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Generalized hyperpigmentation [hp:0007440]
Phenotype [hp:0100334] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007067] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Distal peripheral sensory neuropathy [hp:0007067]
Phenotype [hp:0002524] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001361] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Nystagmus-induced head nodding [hp:0001361]
Phenotype [hp:0000764] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Peripheral axonal degeneration [hp:0000764]
Phenotype [hp:0007105] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006487] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005247] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplasia of the abdominal wall musculature [hp:0005247]
Hypoplasia of the abdominal wall musculature
Phenotype [hp:0009094] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011704] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007922] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypermyelinated retinal fibers [hp:0007922]
Phenotype [hp:0100559] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012254] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007868] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Age-related macular degeneration [hp:0007868]
Phenotype [hp:0004976] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011001] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased bone mineral density [hp:0011001]
Phenotype [hp:0003402] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Decreased miniature endplate potentials [hp:0003402]
Phenotype [hp:0001574] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the integument [hp:0001574]
Phenotype [hp:0001773] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100335] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009005] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Weakness of the intrinsic hand muscles [hp:0009005]
Phenotype [hp:0000422] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the nasal bridge [hp:0000422]
Phenotype [hp:0001430] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the calf musculature [hp:0001430]
Phenotype [hp:0001360] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007229] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Intracerebral periventricular calcifications [hp:0007229]
Intracerebral periventricular calcifications
Phenotype [hp:0000765] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008237] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypothalamic hypothyroidism [hp:0008237]
Phenotype [hp:0007068] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008921] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Neonatal short-limb short stature [hp:0008921]
Phenotype [hp:0007104] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Prolonged somatosensory evoked potentials [hp:0007104]
Prolonged somatosensory evoked potentials
Phenotype [hp:0006262] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Aplasia/Hypoplasia of the 5th finger [hp:0006262]
Phenotype [hp:0011703] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003401] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006992] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Anterior basal encephalocele [hp:0006992]
Phenotype [hp:0004977] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001500] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009839] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Osteolytic defects of the distal phalanges of the hand [hp:0009839]
Osteolytic defects of the distal phalanges of the hand
Phenotype [hp:0009004] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplasia of the musculature [hp:0009004]
Phenotype [hp:0002671] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007107] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Segmental peripheral demyelination [hp:0007107]
Phenotype [hp:0001770] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000762] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Decreased nerve conduction velocity [hp:0000762]
Phenotype [hp:0007069] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Profound static encephalopathy [hp:0007069]
Phenotype [hp:0008922] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Childhood-onset short-trunk short stature [hp:0008922]
Childhood-onset short-trunk short stature
Phenotype [hp:0002526] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Deficit in nonword repetition [hp:0002526]
Phenotype [hp:0009145] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of cerebral artery [hp:0009145]
Phenotype [hp:0001215] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Camptodactyly of 2nd-5th fingers [hp:0001215]
Phenotype [hp:0011158] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004751] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Paroxysmal ventricular tachycardia [hp:0004751]
Phenotype [hp:0006489] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the femoral metaphysis [hp:0006489]
Phenotype [hp:0030148] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003269] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Sudanophilic leukodystrophy [hp:0003269]
Phenotype [hp:0003400] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Basal lamina 'onion bulb' formation [hp:0003400]
Phenotype [hp:0012107] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007920] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Congenital chorioretinal dystrophy [hp:0007920]
Phenotype [hp:0007441] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hyperpigmented/hypopigmented macules [hp:0007441]
Phenotype [hp:0100333] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001501] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0030147] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006165] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Proportionate shortening of all digits [hp:0006165]
Phenotype [hp:0001771] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Achilles tendon contracture [hp:0001771]
Phenotype [hp:0000420] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012108] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Primary open angle glaucoma [hp:0012108]
Phenotype [hp:0002672] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009003] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased subcutaneous truncal adipose tissue [hp:0009003]
Increased subcutaneous truncal adipose tissue
Phenotype [hp:0011309] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001572] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000763] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001216] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Delayed ossification of carpal bones [hp:0001216]
Phenotype [hp:0100396] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Short proximal phalanx of the 4th toe [hp:0100396]
Phenotype [hp:0002527] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005756] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Neonatal epiphyseal stippling [hp:0005756]
Phenotype [hp:0006994] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Diffuse leukoencephalopathy [hp:0006994]
Phenotype [hp:0004979] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007869] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003200] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012687] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010878] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005776] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Carpal bone malsegmentation [hp:0005776]
Phenotype [hp:0005912] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006554] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012811] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004308] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002519] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003049] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Ulnar deviation of the wrist [hp:0003049]
Phenotype [hp:0100703] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002168] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003154] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased circulating ACTH level [hp:0003154]
Phenotype [hp:0002218] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002105] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011999] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004399] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011886] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008784] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Wide capital femoral epiphyses [hp:0008784]
Phenotype [hp:0009735] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001362] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010655] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006829] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002446] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100790] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006818] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006555] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004771] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Premature graying of body hair [hp:0004771]
Phenotype [hp:0012061] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Urinary excretion of sialylated oligosaccharides [hp:0012061]
Urinary excretion of sialylated oligosaccharides
Phenotype [hp:0006769] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011909] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002518] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the periventricular white matter [hp:0002518]
Abnormality of the periventricular white matter
Phenotype [hp:0009164] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormal calcification of the carpal bones [hp:0009164]
Abnormal calcification of the carpal bones
Phenotype [hp:0012810] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010767] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Sacrococcygeal pilonidal abnormality [hp:0010767]
Phenotype [hp:0005162] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Impaired left ventricular function [hp:0005162]
Phenotype [hp:0006473] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Anterior bowing of long bones [hp:0006473]
Phenotype [hp:0002104] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003249] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100702] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003155] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Elevated alkaline phosphatase [hp:0003155]
Phenotype [hp:0002169] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006402] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004398] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010064] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Symphalangism affecting the phalanges of the hallux [hp:0010064]
Symphalangism affecting the phalanges of the hallux
Phenotype [hp:0002217] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002383] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008785] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Delayed ossification of pubic rami [hp:0008785]
Phenotype [hp:0002445] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004309] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001363] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009734] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006817] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Aplasia/Hypoplasia of the cerebellar vermis [hp:0006817]
Aplasia/Hypoplasia of the cerebellar vermis
Phenotype [hp:0012605] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011507] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004306] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the endocardium [hp:0004306]
Phenotype [hp:0006827] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010766] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012251] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006766] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Papillary renal cell carcinoma [hp:0006766]
Phenotype [hp:0007633] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006552] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011440] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Alcohol-induced rhabdomyolysis [hp:0011440]
Phenotype [hp:0005914] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Aplasia/Hypoplasia involving the metacarpal bones [hp:0005914]
Aplasia/Hypoplasia involving the metacarpal bones
Phenotype [hp:0007786] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Lacunar retinal depigmentation [hp:0007786]
Phenotype [hp:0003152] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased serum 1,25-dihydroxyvitamin D3 [hp:0003152]
Increased serum 1,25-dihydroxyvitamin D3
Phenotype [hp:0000548] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002107] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005450] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009737] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002384] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Focal seizures with impairment of consciousness or awareness [hp:0002384]
Focal seizures with impairment of consciousness or awareness
Phenotype [hp:0007431] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Congenital ichthyosiform erythroderma [hp:0007431]
Phenotype [hp:0008711] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Benign prostatic hyperplasia [hp:0008711]
Phenotype [hp:0012606] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007112] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009568] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Aplasia/Hypoplasia of the middle phalanx of the 2nd finger [hp:0009568]
Aplasia/Hypoplasia of the middle phalanx of the 2nd finger
Phenotype [hp:0002444] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005160] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Total anomalous pulmonary venous return [hp:0005160]
Phenotype [hp:0012813] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Unilateral breast hypoplasia [hp:0012813]
Phenotype [hp:0006471] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003048] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011907] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Reduced alpha/beta synthesis ratio [hp:0011907]
Phenotype [hp:0002516] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased intracranial pressure [hp:0002516]
Phenotype [hp:0006767] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Pituitary prolactin cell adenoma [hp:0006767]
Phenotype [hp:0005775] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Multiple skeletal anomalies [hp:0005775]
Phenotype [hp:0007787] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Posterior subcapsular cataract [hp:0007787]
Phenotype [hp:0011441] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the medulla oblongata [hp:0011441]
Phenotype [hp:0006400] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002050] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Macroorchidism, postpubertal [hp:0002050]
Phenotype [hp:0000549] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormal conjugate eye movement [hp:0000549]
Phenotype [hp:0007634] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Nonarteritic anterior ischemic optic neuropathy [hp:0007634]
Nonarteritic anterior ischemic optic neuropathy
Phenotype [hp:0003153] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000437] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009736] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002385] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002219] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008783] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Wide proximal femoral metaphysis [hp:0008783]
Phenotype [hp:0007432] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Intermittent generalized erythematous papular rash [hp:0007432]
Intermittent generalized erythematous papular rash
Phenotype [hp:0002599] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011509] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010765] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002101] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004395] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005452] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Obliteration of frontal sinuses [hp:0005452]
Phenotype [hp:0003150] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0200020] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006978] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Dysmyelinating leukodystrophy [hp:0006978]
Phenotype [hp:0002164] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002442] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011504] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007110] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009566] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Short distal phalanx of the 2nd finger [hp:0009566]
Phenotype [hp:0012608] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008717] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001289] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007437] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Multiple cutaneous leiomyomas [hp:0007437]
Phenotype [hp:0003865] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010874] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000546] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001075] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004394] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006406] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005451] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Decreased cranial base ossification [hp:0005451]
Phenotype [hp:0008780] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Congenital bilateral hip dislocation [hp:0008780]
Phenotype [hp:0000547] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010068] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006765] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002100] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Recurrent aspiration pneumonia [hp:0002100]
Phenotype [hp:0000812] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormal internal genitalia [hp:0000812]
Phenotype [hp:0004305] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002165] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Pterygium formation (nails) [hp:0002165]
Phenotype [hp:0006979] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Sleep-wake cycle disturbance [hp:0006979]
Phenotype [hp:0007438] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Mottled pigmentation of the trunk and proximal extremities [hp:0007438]
Mottled pigmentation of the trunk and proximal extremities
Phenotype [hp:0010650] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Premaxillary underdevelopment [hp:0010650]
Phenotype [hp:0008716] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000121] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100795] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001076] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011883] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001367] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004397] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002103] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002166] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Impaired vibration sensation in the lower limbs [hp:0002166]
Impaired vibration sensation in the lower limbs
Phenotype [hp:0000813] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005165] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009161] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Aplasia/Hypoplasia of the middle phalanx of the 5th finger [hp:0009161]
Aplasia/Hypoplasia of the middle phalanx of the 5th finger
Phenotype [hp:0200022] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008189] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008467] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007548] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Palmoplantar keratosis with erythema and scale [hp:0007548]
Palmoplantar keratosis with erythema and scale
Phenotype [hp:0100792] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012817] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Noncompaction cardiomyopathy [hp:0012817]
Phenotype [hp:0009733] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008715] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011506] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Choroidal neovascularization of the macula [hp:0011506]
Choroidal neovascularization of the macula
Phenotype [hp:0000544] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011884] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormal umbilical stump bleeding [hp:0011884]
Phenotype [hp:0007435] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Diffuse palmoplantar keratoderma [hp:0007435]
Phenotype [hp:0000122] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005453] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Absent/hypoplastic paranasal sinuses [hp:0005453]
Phenotype [hp:0004396] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002167] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Neurological speech impairment [hp:0002167]
Phenotype [hp:0006763] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Anal canal squamous carcinoma [hp:0006763]
Phenotype [hp:0002102] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005164] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009162] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Absent middle phalanx of 5th finger [hp:0009162]
Phenotype [hp:0010769] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004303] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of muscle fibers [hp:0004303]
Phenotype [hp:0010066] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Duplication of phalanx of hallux [hp:0010066]
Phenotype [hp:0200021] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008188] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010982] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007436] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hair-nail ectodermal dysplasia [hp:0007436]
Phenotype [hp:0007549] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Desquamation of skin soon after birth [hp:0007549]
Phenotype [hp:0001591] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011505] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009732] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008714] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002389] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000545] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001369] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007210] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000123] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008897] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Postnatal growth retardation [hp:0008897]
Phenotype [hp:0000277] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the mandible [hp:0000277]
Phenotype [hp:0001132] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000655] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000124] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001071] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Angiokeratoma corporis diffusum [hp:0001071]
Phenotype [hp:0100798] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000920] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Enlargement of the costochondral junction [hp:0000920]
Enlargement of the costochondral junction
Phenotype [hp:0007001] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Loss of Purkinje cells in the cerebellar vermis [hp:0007001]
Loss of Purkinje cells in the cerebellar vermis
Phenotype [hp:0000063] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010760] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007546] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000394] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008608] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypertrophic auricular cartilage [hp:0008608]
Phenotype [hp:0008073] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002160] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006821] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Polymicrogyria, anterior to posterior gradient [hp:0006821]
Polymicrogyria, anterior to posterior gradient
Phenotype [hp:0012534] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001809] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005518] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002055] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Curved linear dimple below the lower lip [hp:0002055]
Curved linear dimple below the lower lip
Phenotype [hp:0005304] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplastic pulmonary veins [hp:0005304]
Phenotype [hp:0005010] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Osteomyelitis leading to amputation due to slow healing fractures [hp:0005010]
Osteomyelitis leading to amputation due to slow healing fractures
Phenotype [hp:0011500] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012068] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003041] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001428] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0200024] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Premature chromatid separation [hp:0200024]
Phenotype [hp:0005381] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Recurrent meningococcal disease [hp:0005381]
Phenotype [hp:0000656] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007321] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Deep white matter hypodensities [hp:0007321]
Phenotype [hp:0008672] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Calcium oxalate nephrolithiasis [hp:0008672]
Phenotype [hp:0001072] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000278] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100799] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001899] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008107] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Plantar crease between first and second toes [hp:0008107]
Plantar crease between first and second toes
Phenotype [hp:0000125] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000064] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007002] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010871] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001133] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010984] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000395] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008607] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Progressive conductive hearing impairment [hp:0008607]
Progressive conductive hearing impairment
Phenotype [hp:0002161] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0200023] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000921] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008072] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Maternal virilization in pregnancy [hp:0008072]
Phenotype [hp:0005305] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012069] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Keratan sulfate excretion in urine [hp:0012069]
Phenotype [hp:0002738] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplastic frontal sinuses [hp:0002738]
Phenotype [hp:0001427] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003042] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011993] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Impaired neutrophil bactericidal activity [hp:0011993]
Impaired neutrophil bactericidal activity
Phenotype [hp:0000126] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001073] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000653] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000396] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002951] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Partial absence of cerebellar vermis [hp:0002951]
Phenotype [hp:0001640] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100796] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007544] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008606] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001134] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000065] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005302] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012532] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011502] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012066] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased urinary disaccharide excretion [hp:0012066]
Increased urinary disaccharide excretion
Phenotype [hp:0008071] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000922] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005458] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Premature closure of fontanelles [hp:0005458]
Phenotype [hp:0002162] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0200026] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001807] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100709] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Reduction of oligodendroglia [hp:0100709]
Phenotype [hp:0004288] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Pseudoepiphyses of hand bones [hp:0004288]
Phenotype [hp:0005661] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011900] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002212] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002057] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100797] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001074] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Atypical nevi in non-sun exposed areas [hp:0001074]
Phenotype [hp:0000127] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000066] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100853] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007545] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Congenital palmoplantar keratosis [hp:0007545]
Phenotype [hp:0000654] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Decreased electroretinogram (ERG) amplitude [hp:0000654]
Decreased electroretinogram (ERG) amplitude
Phenotype [hp:0008297] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Transient hyperphenylalaninemia [hp:0008297]
Phenotype [hp:0001135] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007000] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008605] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Unilateral external ear deformity [hp:0008605]
Phenotype [hp:0009623] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Proximal placement of thumb [hp:0009623]
Phenotype [hp:0008819] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011501] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000923] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005303] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011220] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008070] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012531] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009381] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005384] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Defective B cell activation [hp:0005384]
Phenotype [hp:0003040] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0200025] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001808] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002058] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002211] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008818] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001136] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Retinal arteriolar tortuosity [hp:0001136]
Phenotype [hp:0008078] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003712] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Skeletal muscle hypertrophy [hp:0003712]
Phenotype [hp:0000273] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008102] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Expanded metatarsals with widened medullary cavities [hp:0008102]
Expanded metatarsals with widened medullary cavities
Phenotype [hp:0007542] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Absent pigmentation of the ventral chest [hp:0007542]
Absent pigmentation of the ventral chest
Phenotype [hp:0002109] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001642] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011995] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008675] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Enlarged polycystic ovaries [hp:0008675]
Phenotype [hp:0009626] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Contractures of the interphalangeal joint of the thumb [hp:0009626]
Contractures of the interphalangeal joint of the thumb
Phenotype [hp:0000128] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002059] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011906] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Reduced beta/alpha synthesis ratio [hp:0011906]
Phenotype [hp:0000327] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003359] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0200028] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006558] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Decreased mitochondrial complex III activity in liver tissue [hp:0006558]
Decreased mitochondrial complex III activity in liver tissue
Phenotype [hp:0000659] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002000] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011227] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Elevated C-reactive protein level [hp:0011227]
Phenotype [hp:0006825] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Pallor of dorsal columns of the spinal cord [hp:0006825]
Pallor of dorsal columns of the spinal cord
Phenotype [hp:0003158] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008460] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplastic spinal processes [hp:0008460]
Phenotype [hp:0010659] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Patchy variation in bone mineral density [hp:0010659]
Patchy variation in bone mineral density
Phenotype [hp:0006611] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Decreased number of sternal ossification centers [hp:0006611]
Decreased number of sternal ossification centers
Phenotype [hp:0008462] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001137] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008817] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008103] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Delayed tarsal ossification [hp:0008103]
Phenotype [hp:0003713] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000060] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000274] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007006] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000399] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Prelingual sensorineural hearing impairment [hp:0000399]
Prelingual sensorineural hearing impairment
Phenotype [hp:0001641] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the pulmonary valve [hp:0001641]
Phenotype [hp:0007543] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009738] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the antihelix [hp:0009738]
Phenotype [hp:0008676] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005301] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Persistent left superior vena cava [hp:0005301]
Phenotype [hp:0002213] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003358] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Elevated intracellular cystine [hp:0003358]
Phenotype [hp:0002108] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006559] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006813] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003159] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002448] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000061] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Ambiguous genitalia, female [hp:0000061]
Phenotype [hp:0008572] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001138] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003710] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Exercise-induced muscle cramps [hp:0003710]
Phenotype [hp:0010762] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001644] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002380] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000275] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000657] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002737] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002216] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002002] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006692] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Short chordae tendineae of the tricuspid valve [hp:0006692]
Short chordae tendineae of the tricuspid valve
Phenotype [hp:0011904] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Persistence of hemoglobin F [hp:0011904]
Phenotype [hp:0100659] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the cerebral vasculature [hp:0100659]
Phenotype [hp:0003043] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the shoulder [hp:0003043]
Phenotype [hp:0100858] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000329] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006812] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
White mater abnormalities in the posterior periventricular region [hp:0006812]
White mater abnormalities in the posterior periventricular region
Phenotype [hp:0012062] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004646] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplasia of the nasal bone [hp:0004646]
Phenotype [hp:0004881] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010989] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the intrinsic pathway [hp:0010989]
Phenotype [hp:0010761] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008573] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Low-frequency sensorineural hearing impairment [hp:0008573]
Low-frequency sensorineural hearing impairment
Phenotype [hp:0001139] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000062] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007541] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001643] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001070] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000276] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002381] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006690] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006691] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011998] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006557] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002215] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000658] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0200029] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011903] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003044] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Shoulder flexion contracture [hp:0003044]
Phenotype [hp:0006610] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Wide intermamillary distance [hp:0006610]
Phenotype [hp:0100704] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006824] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011224] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005513] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased megakaryocyte count [hp:0005513]
Phenotype [hp:0005096] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011098] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004872] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000917] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003717] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005523] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Lymphoproliferative disorder [hp:0005523]
Phenotype [hp:0012471] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006693] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005017] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Polyarticular chondrocalcinosis [hp:0005017]
Phenotype [hp:0009088] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Speech articulation difficulties [hp:0009088]
Phenotype [hp:0001814] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003416] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100658] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001290] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002730] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Chronic noninfectious lymphadenopathy [hp:0002730]
Phenotype [hp:0001645] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001701] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000322] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100324] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006067] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Multiple carpal ossification centers [hp:0006067]
Phenotype [hp:0001891] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008069] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000282] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006603] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004871] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000916] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003716] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Generalized muscular appearance from birth [hp:0003716]
Generalized muscular appearance from birth
Phenotype [hp:0003302] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004987] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006172] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Flattened, squared-off epiphyses of tubular bones [hp:0006172]
Flattened, squared-off epiphyses of tubular bones
Phenotype [hp:0100299] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Muscle fiber inclusion bodies [hp:0100299]
Phenotype [hp:0001700] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009417] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Pseudoepiphyses of the 3rd finger [hp:0009417]
Phenotype [hp:0002731] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Defective lymphocyte apoptosis [hp:0002731]
Phenotype [hp:0001646] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the aortic valve [hp:0001646]
Phenotype [hp:0001892] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000059] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007009] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Central nervous system degeneration [hp:0007009]
Phenotype [hp:0000860] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007328] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003795] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Short middle phalanx of toe [hp:0003795]
Phenotype [hp:0003715] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012473] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002958] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001647] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003305] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006695] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Atrioventricular canal defect [hp:0006695]
Phenotype [hp:0001812] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005521] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Disseminated intravascular coagulation [hp:0005521]
Phenotype [hp:0100326] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Immunologic hypersensitivity [hp:0100326]
Phenotype [hp:0002732] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006174] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Metacarpal diaphyseal endosteal sclerosis [hp:0006174]
Metacarpal diaphyseal endosteal sclerosis
Phenotype [hp:0003528] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000324] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006069] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Severe carpal ossification delay [hp:0006069]
Phenotype [hp:0003418] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010530] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008678] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007327] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Mixed demyelinating and axonal polyneuropathy [hp:0007327]
Mixed demyelinating and axonal polyneuropathy
Phenotype [hp:0002669] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011228] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000284] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the ocular region [hp:0000284]
Phenotype [hp:0012539] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008823] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplastic inferior pubic rami [hp:0008823]
Phenotype [hp:0001780] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006696] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Polymorphic and polytopic ventricular extrasystoles [hp:0006696]
Polymorphic and polytopic ventricular extrasystoles
Phenotype [hp:0002959] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Impaired Ig class switch recombination [hp:0002959]
Phenotype [hp:0001648] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003304] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003417] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000918] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003529] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Parathormone-independent increased renal tubular calcium reabsorption [hp:0003529]
Parathormone-independent increased renal tubular calcium reabsorption
Phenotype [hp:0007007] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Cavitation of the basal ganglia [hp:0007007]
Phenotype [hp:0002733] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the lymph nodes [hp:0002733]
Phenotype [hp:0001894] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100327] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008677] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Congenital nephrotic syndrome [hp:0008677]
Phenotype [hp:0000325] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001291] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the cranial nerves [hp:0001291]
Phenotype [hp:0010493] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007326] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Progressive choreoathetosis [hp:0007326]
Phenotype [hp:0003797] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008358] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000283] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011229] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008824] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004876] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Spontaneous neonatal pneumothorax [hp:0004876]
Phenotype [hp:0012248] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003526] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001818] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012322] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006830] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Severe neonatal hypotonia in males [hp:0006830]
Phenotype [hp:0005386] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Recurrent protozoan infections [hp:0005386]
Phenotype [hp:0001649] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000913] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011094] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007850] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Retinal vascular proliferation [hp:0007850]
Phenotype [hp:0000758] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Impaired use of nonverbal behaviors [hp:0000758]
Phenotype [hp:0012182] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Oropharyngeal squamous cell carcinoma [hp:0012182]
Phenotype [hp:0003362] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased circulating very-low-density lipoprotein cholesterol [hp:0003362]
Increased circulating very-low-density lipoprotein cholesterol
Phenotype [hp:0009843] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Aplasia/Hypoplasia of the middle phalanges of the hand [hp:0009843]
Aplasia/Hypoplasia of the middle phalanges of the hand
Phenotype [hp:0006608] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012537] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002667] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Nephroblastoma (Wilms tumor) [hp:0002667]
Phenotype [hp:0000863] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003798] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008357] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Reduced factor XIII activity [hp:0008357]
Phenotype [hp:0007325] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004280] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Irregular ossification of hand bones [hp:0004280]
Phenotype [hp:0100654] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000652] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100541] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008821] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001895] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001141] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001423] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
X-linked dominant inheritance [hp:0001423]
Phenotype [hp:0001817] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011372] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011910] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Shortening of all phalanges of fingers [hp:0011910]
Phenotype [hp:0003527] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012321] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
D-2-hydroxyglutaric aciduria [hp:0012321]
Phenotype [hp:0006698] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005387] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000759] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormal peripheral nervous system morphology [hp:0000759]
Abnormal peripheral nervous system morphology
Phenotype [hp:0003250] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000912] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003363] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008822] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplastic ischiopubic rami [hp:0008822]
Phenotype [hp:0005090] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009844] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Broad middle phalanx of finger [hp:0009844]
Phenotype [hp:0003799] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008356] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002668] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002880] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000864] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the hypothalamus-pituitary axis [hp:0000864]
Abnormality of the hypothalamus-pituitary axis
Phenotype [hp:0003419] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001896] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002953] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Vertebral compression fractures [hp:0002953]
Phenotype [hp:0030022] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000651] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000055] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of female external genitalia [hp:0000055]
Abnormality of female external genitalia
Phenotype [hp:0100852] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormal fear/anxiety-related behavior [hp:0100852]
Phenotype [hp:0001140] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007917] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Tractional retinal detachment [hp:0007917]
Phenotype [hp:0100540] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004283] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004878] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Intercostal muscle weakness [hp:0004878]
Phenotype [hp:0003301] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Irregular vertebral endplates [hp:0003301]
Phenotype [hp:0003524] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Decreased methionine synthase activity [hp:0003524]
Phenotype [hp:0001816] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011096] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000915] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Pectus excavatum of inferior sternum [hp:0000915]
Phenotype [hp:0012180] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003719] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005011] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006699] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Ectopic supraventricular rhythms [hp:0006699]
Phenotype [hp:0004980] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003251] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000280] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008242] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002665] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0009845] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Bullet-shaped middle phalanges of the hand [hp:0009845]
Bullet-shaped middle phalanges of the hand
Phenotype [hp:0010164] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Cone-shaped epiphyses of the toes [hp:0010164]
Phenotype [hp:0000320] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001425] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000650] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Reduced amplitude of pattern visual evoked potentials [hp:0000650]
Reduced amplitude of pattern visual evoked potentials
Phenotype [hp:0001897] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005389] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Depletion of components of the alternative complement pathway [hp:0005389]
Depletion of components of the alternative complement pathway
Phenotype [hp:0008890] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100923] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003300] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000914] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003252] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Anteriorly displaced genitalia [hp:0003252]
Phenotype [hp:0003365] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011097] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002220] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Melanin pigment aggregation in hair shafts [hp:0002220]
Melanin pigment aggregation in hair shafts
Phenotype [hp:0000866] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Euthyroid multinodular goiter [hp:0000866]
Phenotype [hp:0005092] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Streaky metaphyseal sclerosis [hp:0005092]
Phenotype [hp:0002666] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008354] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Factor X activation deficiency [hp:0008354]
Phenotype [hp:0000321] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100651] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001426] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001142] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002882] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000057] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008108] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Advanced tarsal ossification [hp:0008108]
Phenotype [hp:0001898] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased red blood cell mass [hp:0001898]
Phenotype [hp:0002955] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002883] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001786] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100545] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010275] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Pseudoepiphyses of the proximal phalanges of the hand [hp:0010275]
Pseudoepiphyses of the proximal phalanges of the hand
Phenotype [hp:0100650] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000543] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008353] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001581] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012806] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008708] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Partial development of the penile shaft [hp:0008708]
Phenotype [hp:0008198] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Congenital hypoparathyroidism [hp:0008198]
Phenotype [hp:0002663] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Delayed epiphyseal ossification [hp:0002663]
Phenotype [hp:0002510] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001298] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007052] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Multifocal cerebral white matter abnormalities [hp:0007052]
Multifocal cerebral white matter abnormalities
Phenotype [hp:0000867] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Secondary hyperparathyroidism [hp:0000867]
Phenotype [hp:0011447] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hyposegmentation of neutrophil nuclei [hp:0011447]
Phenotype [hp:0004313] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008197] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Absence of pubertal development [hp:0008197]
Phenotype [hp:0000804] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001709] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Third degree atrioventricular block [hp:0001709]
Phenotype [hp:0003635] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Loss of subcutaneous adipose tissue in limbs [hp:0003635]
Loss of subcutaneous adipose tissue in limbs
Phenotype [hp:0011800] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007854] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Glaucomatous visual field defect [hp:0007854]
Phenotype [hp:0004390] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000542] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100544] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002884] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007215] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Periodic hyperkalemic paralysis [hp:0007215]
Phenotype [hp:0002450] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormal motor neuron morphology [hp:0002450]
Phenotype [hp:0010499] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001297] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002511] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001580] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Pigmented micronodular adrenocortical disease [hp:0001580]
Pigmented micronodular adrenocortical disease
Phenotype [hp:0002664] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100291] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of central somatosensory evoked potentials [hp:0100291]
Abnormality of central somatosensory evoked potentials
Phenotype [hp:0011090] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008247] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Euthyroid hyperthyroxinemia [hp:0008247]
Phenotype [hp:0007054] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002378] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000868] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Decreased fertility in females [hp:0000868]
Phenotype [hp:0007780] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Cortical pulverulent cataract [hp:0007780]
Phenotype [hp:0000803] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011165] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012185] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Constrictive median neuropathy [hp:0012185]
Phenotype [hp:0006986] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007913] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Reticular retinal dystrophy [hp:0007913]
Phenotype [hp:0011801] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Enlargement of parotid gland [hp:0011801]
Phenotype [hp:0002805] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Accelerated bone age after puberty [hp:0002805]
Phenotype [hp:0010535] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007293] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Anterior sacral meningocele [hp:0007293]
Phenotype [hp:0001708] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004879] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Intermittent hyperventilation [hp:0004879]
Phenotype [hp:0012245] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100543] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002661] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Painless fractures due to injury [hp:0002661]
Phenotype [hp:0001788] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Premature rupture of membranes [hp:0001788]
Phenotype [hp:0010168] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Ivory epiphyses of the toes [hp:0010168]
Phenotype [hp:0002885] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000541] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005807] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011449] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008706] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Distal urethral duplication [hp:0008706]
Phenotype [hp:0001583] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005168] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Elevated right atrial pressure [hp:0005168]
Phenotype [hp:0006253] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Swelling of proximal interphalangeal joints [hp:0006253]
Swelling of proximal interphalangeal joints
Phenotype [hp:0012184] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006335] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Persistence of primary teeth [hp:0006335]
Phenotype [hp:0000869] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002110] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000756] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012246] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004540] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Congenital, generalized hypertrichosis [hp:0004540]
Phenotype [hp:0004392] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0010538] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007700] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Anterior segment dysgenesis [hp:0007700]
Phenotype [hp:0004311] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002804] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Arthrogryposis multiplex congenita [hp:0002804]
Phenotype [hp:0006060] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Tombstone-shaped proximal phalanges [hp:0006060]
Phenotype [hp:0100542] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormal localization of kidney [hp:0100542]
Phenotype [hp:0000430] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002886] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000540] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001789] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011448] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100293] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001582] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008245] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006254] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000805] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012183] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hyperplastic colonic polyposis [hp:0012183]
Phenotype [hp:0000757] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002111] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Restrictive respiratory insufficiency [hp:0002111]
Phenotype [hp:0006334] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplasia of the primary teeth [hp:0006334]
Phenotype [hp:0004768] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003521] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Disproportionate short-trunk short stature [hp:0003521]
Disproportionate short-trunk short stature
Phenotype [hp:0006984] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Distal sensory loss of all modalities [hp:0006984]
Phenotype [hp:0003634] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001706] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003256] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the coagulation cascade [hp:0003256]
Phenotype [hp:0007915] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Polymorphous posterior corneal dystrophy [hp:0007915]
Polymorphous posterior corneal dystrophy
Phenotype [hp:0010537] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002803] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005917] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Supernumerary metacarpal bones [hp:0005917]
Phenotype [hp:0000750] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Delayed speech and language development [hp:0000750]
Phenotype [hp:0008789] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Cone-shaped capital femoral epiphysis [hp:0008789]
Phenotype [hp:0007057] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002514] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001371] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001810] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007430] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006176] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Two carpal ossification centers present at birth [hp:0006176]
Two carpal ossification centers present at birth
Phenotype [hp:0003639] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Elevated urinary epinephrine [hp:0003639]
Phenotype [hp:0001782] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000431] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007858] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000808] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0004763] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Paroxysmal supraventricular tachycardia [hp:0004763]
Phenotype [hp:0003307] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001705] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Right ventricular outlet obstruction [hp:0001705]
Phenotype [hp:0008193] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Primary gonadal insufficiency [hp:0008193]
Phenotype [hp:0005769] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Fifth finger distal phalanx clinodactyly [hp:0005769]
Fifth finger distal phalanx clinodactyly
Phenotype [hp:0011379] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Dilated vestibule of the inner ear [hp:0011379]
Phenotype [hp:0012240] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased intramyocellular lipid droplets [hp:0012240]
Increased intramyocellular lipid droplets
Phenotype [hp:0006251] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006477] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the alveolar ridges [hp:0006477]
Phenotype [hp:0007058] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Generalized cerebral atrophy/hypoplasia [hp:0007058]
Phenotype [hp:0008935] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Generalized neonatal hypotonia [hp:0008935]
Phenotype [hp:0010270] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Cone-shaped epiphyses of the proximal phalanges of the hand [hp:0010270]
Cone-shaped epiphyses of the proximal phalanges of the hand
Phenotype [hp:0001370] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000751] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001204] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Distal symphalangism (hands) [hp:0001204]
Phenotype [hp:0002515] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008788] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Delayed pubic bone ossification [hp:0008788]
Phenotype [hp:0100321] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the dentate nucleus [hp:0100321]
Phenotype [hp:0001783] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0002888] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006064] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Limited interphalangeal movement [hp:0006064]
Phenotype [hp:0009085] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003258] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003411] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Proximal femoral metaphyseal irregularity [hp:0003411]
Proximal femoral metaphyseal irregularity
Phenotype [hp:0010539] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0100548] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005234] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Neonatal intestinal obstruction [hp:0005234]
Phenotype [hp:0012189] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001704] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003306] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006332] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Supernumerary maxillary incisor [hp:0006332]
Phenotype [hp:0005768] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
2-4 toe cutaneous syndactyly [hp:0005768]
Phenotype [hp:0005099] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012241] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Levator palpebrae superioris atrophy [hp:0012241]
Phenotype [hp:0005999] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0011169] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Generalized clonic seizures [hp:0011169]
Phenotype [hp:0000807] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006252] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Interphalangeal joint erosions [hp:0006252]
Phenotype [hp:0004762] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Hypoplasia of right ventricle [hp:0004762]
Phenotype [hp:0002512] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001373] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000752] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007299] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Dysfunction of lateral corticospinal tracts [hp:0007299]
Dysfunction of lateral corticospinal tracts
Phenotype [hp:0001587] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007117] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Corticospinal tract atrophy [hp:0007117]
Phenotype [hp:0003309] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Ovoid thoracolumbar vertebrae [hp:0003309]
Phenotype [hp:0003414] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012188] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0007910] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Nonprogressive congenital retinal dystrophy [hp:0007910]
Nonprogressive congenital retinal dystrophy
Phenotype [hp:0007856] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Punctate opacification of the cornea [hp:0007856]
Phenotype [hp:0002808] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005235] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0005019] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003259] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0012242] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008191] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0008249] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001890] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Autoimmune hemolytic anemia [hp:0001890]
Phenotype [hp:0009951] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Partial duplication of the distal phalanx of the 2nd finger [hp:0009951]
Partial duplication of the distal phalanx of the 2nd finger
Phenotype [hp:0001586] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001785] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0003308] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0000434] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Nasal mucosa telangiectasia [hp:0000434]
Phenotype [hp:0008786] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0006179] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Pseudoepiphyses of second metacarpal [hp:0006179]
Phenotype [hp:0010497] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Phenotype [hp:0001702] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Abnormality of the tricuspid valve [hp:0001702]
Phenotype [hp:0006980] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Progressive leukoencephalopathy [hp:0006980]
Phenotype [hp:0004764] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Myxomatous mitral valve degeneration [hp:0004764]
Phenotype [hp:0006758] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Malignant genitourinary tract tumor [hp:0006758]
Phenotype [hp:0005766] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Disproportionate shortening of the tibia [hp:0005766]
Disproportionate shortening of the tibia
Phenotype [hp:0012187] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Increased erythrocyte protoporphyrin concentration [hp:0012187]
Increased erythrocyte protoporphyrin concentration
Phenotype [hp:0005997] from the Human Phenotype Ontology (HPO). Phenotypes are identified by the HPO ID. HPID-UMLS cross-references extracted from the 2015-06-20 HPO release.
Restricted neck movement due to contractures [hp:0005997]
Restricted neck movement due to contractures