Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal forearm bone morphology (HP:0040072)

Grandparent Node:
Exostoses (HP:0100777)

Parent Node:
Abnormal morphology of the radius (HP:0002818)

Parent Node:
Exostoses of the forearm bones (HP:0003960)

..Starting node
..Exostoses of the radius (HP:0003986)

Term ID:

3986

Name:

Exostoses of the radius

Synonym:

Definition:

Comments:

Reference:

HP:0003986

Genes and Diseases:

Child Nodes:

........

Exostoses of the radial metaphysis (HP:0004017)

Sister Nodes:

Exostoses of the ulna (HP:0003985)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0003986	HP:0003986	Exostoses of the radius	0	CL E G H
HP:0003986	HP:0004017	Exostoses of the radial metaphysis	1	CL E G H

Genes (0) :

Diseases (0) :

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.