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DO Term : hypertrophic cardiomyopathy 20 [DOID:0110326] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1.

synonyms:
cardiomyopathy familial hypertrophic 20,
613876,
CMH20,
OMIM:613876

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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