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DOID:0050431 - arrhythmogenic right ventricular cardiomyopathy
Disease Ontology Definition:An intrinsic cardiomyopathy that is characterized by hypokinetic areas involving the free wall of the right ventricle, with fibrofatty replacement of the right ventricular myocardium, with associated arrhythmias originating in the right ventricle and limited or no involvement of the left ventricle.
Synonyms: arrhythmogenic right ventricular dysplasia, arrhythmogenic right ventricular dysplasia/cardiomyopathy, ARVC, ARVC cardiomyopathy, ARVD, right ventricular ACM
Xenbase Genes : jup, dsp, tmem43, dsg2, pkp2
MONDO:0016587 - arrhythmogenic right ventricular cardiomyopathy |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
intrinsic cardiomyopathy (is_a)