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 jaw muscles (HP:0045037)

Parent Node:
Abnormality of masticatory muscle (HP:0410011)

..Starting node
..Abnormality of lateral pterygoid muscle (HP:3000068)

Term ID:

3000068

Name:

Abnormality of lateral pterygoid muscle

Synonym:

Definition:

An abnormality of a lateral pterygoid muscle.

Comments:

Reference:

HP:3000068

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormality of masseter muscle (HP:3000005)

Abnormality of medial pterygoid muscle (HP:3000006)

Abnormality of temporalis muscle (HP:3000017)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:3000068	HP:3000068	Abnormality of lateral pterygoid 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.