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DO Term : familial restrictive cardiomyopathy 3 [DOID:0111427] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNT2 gene on chromosome 1q32.1.

synonyms:
restrictive cardiomyopathy 3,
RCM3,
OMIM:612422,
612422

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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