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Summary Literature (0)
MIM:612422 - CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3; RCM3

Xenbase Genes: tnnt2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012900 - cardiomyopathy, familial restrictive, 3
MONDO:0019150 - obsolete familial isolated restrictive cardiomyopathy

Disease Ontology (DO):
DOID:0111427 - restrictive cardiomyopathy 3
DOID:397 - restrictive cardiomyopathy