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familial cardiomyopathy

Disease Summary
Associated Targets (1057)
Tbio

751

Tchem

171

Tclin

74

Tdark

61


Mondo Description An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome.
Mondo Term and Equivalent IDs
MONDO:0005217:  familial cardiomyopathy
EFO:0002945: 
SCTID:35728003: 
UMLS:C0264789: