restrictive cardiomyopathy 3 Disease Ontology Browser

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Disease Ontology Browser

restrictive cardiomyopathy 3 (DOID:0111427)
Alliance: disease page
Synonyms: familial restrictive cardiomyopathy 3; RCM3
Alt IDs: OMIM:612422
Definition: A restrictive cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNT2 gene on chromosome 1q32.1.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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