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DO Term : hypertrophic cardiomyopathy 21 [DOID:0110311] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial hypertrophic cardiomyopathy associated that has_material_basis_in region 7p12.1-q21 variation.

synonyms:
OMIM:614676,
614676,
cardiomyopathy familial hypertrophic 21,
CMH21

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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