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DO Term : hypertrophic cardiomyopathy 7 [DOID:0110313] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.

synonyms:
613690,
cardiomyopathy, familial hypertrophic 7,
OMIM:613690,
CMH7

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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