Any familial isolated restrictive cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
cardiomyopathy, familial restrictive, 1
MONDO:0007270
Gaucher disease type I
MONDO:0009265
glycogen storage disease II
MONDO:0009290
Hurler syndrome
MONDO:0011758
idiopathic hypereosinophilic syndrome
MONDO:0011895
cardiomyopathy, familial restrictive, 2
MONDO:0012306