Human Phenotype Ontology

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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 upper limb (HP:0002817)

Grandparent Node:
Asymmetric growth (HP:0100555)

Parent Node:
Hemiatrophy (HP:0100556)

Parent Node:
Upper limb asymmetry (HP:0100560)

..Starting node
..Hemiatrophy of upper limb (HP:0100558)

Term ID:

100558

Name:

Hemiatrophy of upper limb

Synonym:

Asymmetric upper limb shortening; Hemihypotrophy of upper limb

Definition:

Unilateral atrophy (reduction in size) of an arm.

Comments:

Reference:

HP:0100558

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hemihypertrophy of upper limb (HP:0100554)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100558	HP:0100558	Hemiatrophy of upper 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.