Dilated cardiomyopathy 2A

MONDO:0012746

A dilated cardiomyopathy that has material basis in mutation in the TNNI3 gene on chromosome 19q13.

Also known as: CMD2A, cardiomyopathy, dilated, type 2A, dilated cardiomyopathy type 2A, cardiomyopathy, congestive, autosomal recessive, cardiomyopathy, dilated, 2A, cardiomyopathy, dilated, autosomal recessive

8 clinical trials for this condition and its sub-types, 0 tagged with Dilated cardiomyopathy 2A itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by