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, primary restrictive cardiomyopathy (disorder), Restrictive cardiomyopathy, Restrictive cardiomyopathy (disorder), primary restrictive cardiomyopathy

Echinobase Genes :


MIM:

MIM:115210 - cardiomyopathy, familial restrictive, 1; rcm1

MIM:612422 - cardiomyopathy, familial restrictive, 3; rcm3

MIM:615248 - cardiomyopathy, dilated, 1kk; cmd1kk cardiomyopathy, familial hypertrophic, 22, included; cmh22, included;; cardiomyopathy, familial restrictive, 4, included; rcm4, included

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee