Dilated cardiomyopathy 1AA

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the ACTN2 gene.

Also known as: ACTN2 familial isolated dilated cardiomyopathy, CMD1AA, cardiomyopathy, dilated, 1AA, with or without LVNC, cardiomyopathy, hypertrophic, 23, with or without LVNC, dilated cardiomyopathy type 1AA, familial isolated dilated cardiomyopathy caused by mutation in ACTN2, cardiomyopathy, dilated, 1AA, with or without left ventricular noncompaction, cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction

8 clinical trials for this condition and its sub-types, 0 tagged with Dilated cardiomyopathy 1AA itself.