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Summary Literature (0)
DOID:0111427 - familial restrictive cardiomyopathy 3

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

Synonyms: familial restrictive cardiomyopathy 3, RCM3, restrictive cardiomyopathy 3

Xenbase Genes : tnnt2


MIM:
MIM:612422 - CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3; RCM3

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): restrictive cardiomyopathy (is_a)