Hypertrophic cardiomyopathy 2

MONDO:0007266

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene.

Also known as: CMH2, TNNT2 hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, type 2, cardiomyopathy, hypertrophic, 2, familial hypertrophic cardiomyopathy type 2, hypertrophic cardiomyopathy 2, hypertrophic cardiomyopathy caused by mutation in TNNT2, hypertrophic cardiomyopathy type 2

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 2 itself.

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Part of

↑ Familial hypertrophic cardiomyopathy (86) ↑ TNNT2-related cardiomyopathy (0)

Including sub-types (8) Tagged with Hypertrophic cardiomyopathy 2 (0)

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