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Summary Literature (0)
DOID:397 - restrictive cardiomyopathy


Disease Ontology Definition:An intrinsic cardiomyopathy characterized by impaired ventricular filling, with normal or decreased diastolic volume of either or both ventricles typically resulting from increased stiffness of the myocardium.

Synonyms: Cardiomyopathy, constrictive, Familial restrictive cardiomyopathy, Restrictive cardiomyopathy, Restrictive cardiomyopathy (disorder), primary restrictive cardiomyopathy, primary restrictive cardiomyopathy (disorder)

In OMIM:
OMIM:115210 - CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1; RCM1
OMIM:612422 - CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3; RCM3
OMIM:615248 - CARDIOMYOPATHY, DILATED, 1KK; CMD1KK

In Mondo Disease Ontology:
MONDO:0005201 - restrictive cardiomyopathy

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : tnnt2, tnni3, mypn

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): intrinsic cardiomyopathy (is_a)