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 facial musculature (HP:0000301)

Parent Node:
Abnormal cheek morphology (HP:0004426)

Parent Node:
Abnormality of muscle of facial expression (HP:0430019)

..Starting node
..Abnormality of zygomaticus major muscle (HP:3000018)

Term ID:

3000018

Name:

Abnormality of zygomaticus major muscle

Synonym:

Definition:

An abnormality of a zygomaticus major muscle.

Comments:

Reference:

HP:3000018

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormality of depressor anguli oris muscle (HP:3000028)

Abnormality of depressor labii inferioris (HP:3000029)

Abnormality of levator anguli oris (HP:3000070)

Abnormality of levator labii superioris (HP:3000071)

Abnormality of levator labii superioris alaeque nasi muscle (HP:0430020)

Abnormality of mentalis muscle (HP:3000007)

Abnormality of orbicularis oris muscle (HP:3000010)

Abnormality of risorius muscle (HP:3000015)

Abnormality of zygomaticus minor muscle (HP:3000020)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:3000018	HP:3000018	Abnormality of zygomaticus major muscle	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.