Hypertrophic cardiomyopathy 20

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

Also known as: CMH20, NEXN hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, type 20, cardiomyopathy, hypertrophic, 20, hypertrophic cardiomyopathy caused by mutation in NEXN, hypertrophic cardiomyopathy type 20, cardiomyopathy, familial hypertrophic, 20

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 20 itself.