An instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome.
Comprehensive, easy-to-understand information about this condition
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endomyocardial fibrosis
MONDO:0006746
cardiomyopathy, familial restrictive, 1
MONDO:0007270
Gaucher disease type I
MONDO:0009265
glycogen storage disease II
MONDO:0009290
Naxos disease
MONDO:0011017
Hurler syndrome
MONDO:0011758