has characteristic has characteristic restrictive cardiomyopathy familial cardiomyopathy familial restrictive cardiomyopathy https://github.com/monarch-initiative/mondo/issues/7693 GARD:0020532 MEDGEN:468561 MONDO:0016340 SCTID:233878008 UMLS:C0340429 ICD9:425.4 Orphanet:217635 OMIMPS:115210 An instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome. hereditary restrictive cardiomyopathy inherited