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DO Term : familial restrictive cardiomyopathy 2 [DOID:0111426] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A restrictive cardiomyopathy that has_material_basis_in variation in a region on chromosome 10q23.3.

synonyms:
RCM2,
OMIM:609578,
restrictive cardiomyopathy 2,
609578

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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