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:
Upper limb muscle hypoplasia (HP:0009016)

Parent Node:
Aplasia/Hypoplasia of the triceps (HP:0009784)

Parent Node:
Hypoplasia of the upper arm musculature (HP:0030239)

..Starting node
..Triceps hypoplasia (HP:0100855)

Term ID:

100855

Name:

Triceps hypoplasia

Synonym:

Small triceps; Underdeveloped triceps

Definition:

Hypoplasia of the triceps muscle.

Comments:

Reference:

HP:0100855

Genes and Diseases:

Child Nodes:

Sister Nodes:

Biceps hypoplasia (HP:0009007)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100855	HP:0100855	Triceps hypoplasia	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.