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 tongue muscle (HP:0040173)

Parent Node:
Abnormality of extrinsic muscle of tongue (HP:0040174)

..Starting node
..Abnormality of styloglossus muscle (HP:3000016)

Term ID:

3000016

Name:

Abnormality of styloglossus muscle

Synonym:

Definition:

An abnormality of the styloglossus muscle.

Comments:

Reference:

HP:3000016

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormality of genioglossus muscle (HP:3000045)

Abnormality of palatoglossus muscle (HP:3000011)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:3000016	HP:3000016	Abnormality of styloglossus 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.