Cardiomyopathy, familial restrictive, 1

MONDO:0007270

Any familial isolated restrictive cardiomyopathy in which the cause of the disease is a mutation in the TNNI3 gene.

Also known as: TNNI3 familial isolated restrictive cardiomyopathy, cardiomyopathy, familial restrictive, 1, cardiomyopathy, familial restrictive, type 1, familial isolated restrictive cardiomyopathy caused by mutation in TNNI3, RCM1, Rcm

8 clinical trials for this condition and its sub-types, 0 tagged with Cardiomyopathy, familial restrictive, 1 itself.

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↑ Familial restrictive cardiomyopathy (62)

Including sub-types (8) Tagged with Cardiomyopathy, familial restrictive, 1 (0)

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