Hypertrophic cardiomyopathy 17

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the JPH2 gene.

Also known as: CMH17, JPH2 hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, type 17, cardiomyopathy, hypertrophic, 17, hypertrophic cardiomyopathy caused by mutation in JPH2, hypertrophic cardiomyopathy type 17, cardiomyopathy, familial hypertrophic, 17

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 17 itself.