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 soft palate morphology (HP:0100736)

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

Parent Node:
Abnormality of musculature of soft palate (HP:0430014)

..Starting node
..Abnormality of tensor veli palatini muscle (HP:0430016)

Term ID:

430016

Name:

Abnormality of tensor veli palatini muscle

Synonym:

Definition:

An abnormality of the tensor veli palatini muscle

Comments:

Reference:

HP:0430016

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormality of levator veli palatini muscle (HP:3000073)

Abnormality of palatoglossus muscle (HP:3000011)

Abnormality of palatopharyngeus muscle (HP:3000012)

Abnormality of uvular muscle (HP:0430017)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0430016	HP:0430016	Abnormality of tensor veli palatini 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.