Hypertrophic cardiomyopathy 6

MONDO:0010946

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the PRKAG2 gene.

Also known as: CMH6, PRKAG2 hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, type 6, cardiomyopathy, hypertrophic 6, hypertrophic cardiomyopathy 6, hypertrophic cardiomyopathy caused by mutation in PRKAG2, hypertrophic cardiomyopathy type 6, cardiomyopathy, familial hypertrophic, 6

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 6 itself.

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Part of

↑ Familial hypertrophic cardiomyopathy (85) ↑ PRKAG2-related cardiomyopathy (4)

Including sub-types (8) Tagged with Hypertrophic cardiomyopathy 6 (0)

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