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DO Term : hypertrophic cardiomyopathy 14 [DOID:0110320] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial hypertrophic cardiomyopathy that has_material_basis_in mutation in the MYH6 gene.

synonyms:
cardiomyopathy familial hypertrophic 14,
613251,
OMIM:613251,
CMH14

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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