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DO Term : hypertrophic cardiomyopathy 1 [DOID:0110307] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12.

synonyms:
hypertrophic cardiomyopathy 19,
CMH1,
cardiomyopathy, familial hypertrophic 1,
DOID:0110325,
192600,
OMIM:192600

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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