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 upper limb (HP:0002817)

Grandparent Node:
Asymmetric growth (HP:0100555)

Parent Node:
Hemihypertrophy (HP:0001528)

Parent Node:
Hypertrophy of the upper limb (HP:0010484)

Parent Node:
Upper limb asymmetry (HP:0100560)

..Starting node
..Hemihypertrophy of upper limb (HP:0100554)

Term ID:

100554

Name:

Hemihypertrophy of upper limb

Synonym:

Overgrowth of one arm

Definition:

Overgrowth of only one arm.

Comments:

Reference:

HP:0100554

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hemiatrophy of upper limb (HP:0100558)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100554	HP:0100554	Hemihypertrophy 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.