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DO Term : hypertrophic cardiomyopathy 8 [DOID:0110314] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial hypertrophic cardiomyopathy that has_material_basis_in homozygous or heterozygous mutation in the MYL3 gene.

synonyms:
cardiomyopathy, familial hypertrophic, 8,
OMIM:608751,
cardiomyopathy hypertrophic mid-left ventricular chamber type 1,
608751

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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