Hypertrophic cardiomyopathy 18

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

Also known as: CMH18, PLN hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, type 18, cardiomyopathy, hypertrophic, 18, hypertrophic cardiomyopathy caused by mutation in PLN, hypertrophic cardiomyopathy type 18, cardiomyopathy, familial hypertrophic, 18

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 18 itself.