Cardiomyopathy, familial restrictive, 3

MONDO:0012900

Any familial isolated restrictive cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene.

Also known as: TNNT2 familial isolated restrictive cardiomyopathy, cardiomyopathy, familial restrictive, 3, cardiomyopathy, familial restrictive, type 3, familial isolated restrictive cardiomyopathy caused by mutation in TNNT2, RCM3

8 clinical trials for this condition and its sub-types, 0 tagged with Cardiomyopathy, familial restrictive, 3 itself.

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↑ Familial restrictive cardiomyopathy (62) ↑ TNNT2-related cardiomyopathy (0)

Including sub-types (8) Tagged with Cardiomyopathy, familial restrictive, 3 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.