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:
Abnormal tongue morphology (HP:0030809)

Grandparent Node:
Abnormality of the musculature (HP:0003011)

Parent Node:
Abnormality of the tongue muscle (HP:0040173)

..Starting node
..Abnormality of extrinsic muscle of tongue (HP:0040174)

Term ID:

40174

Name:

Abnormality of extrinsic muscle of tongue

Synonym:

Abnormality of extrinsic lingual muscle

Definition:

Comments:

Reference:

HP:0040174

Genes and Diseases:

Child Nodes:

........

Abnormality of palatoglossus muscle (HP:3000011)

........

Abnormality of styloglossus muscle (HP:3000016)

........

Abnormality of genioglossus muscle (HP:3000045)

Sister Nodes:

Abnormality of intrinsic muscle of tongue (HP:3000064)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040174	HP:0040174	Abnormality of extrinsic muscle of tongue	0	CL E G H
HP:0040174	HP:3000045	Abnormality of genioglossus muscle	1	CL E G H
HP:0040174	HP:3000016	Abnormality of styloglossus muscle	1	CL E G H
HP:0040174	HP:3000011	Abnormality of palatoglossus muscle	1	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.