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:
Abnormality of the lower limb (HP:0002814)

Grandparent Node:
Asymmetric growth (HP:0100555)

Parent Node:
Hemiatrophy (HP:0100556)

Parent Node:
Lower limb asymmetry (HP:0100559)

..Starting node
..Hemiatrophy of lower limb (HP:0100557)

Term ID:

100557

Name:

Hemiatrophy of lower limb

Synonym:

Asymmetric lower limb shortening

Definition:

Unilateral atrophy (reduction in size) of a leg.

Comments:

Reference:

HP:0100557

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hemihypertrophy of lower limb (HP:0100553)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100557	HP:0100557	Hemiatrophy of lower limb	0	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.