Dilated cardiomyopathy 1G

MONDO:0011400

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

Also known as: CMD1G, TTN familial isolated dilated cardiomyopathy, cardiomyopathy, dilated, type 1G, dilated cardiomyopathy type 1G, familial isolated dilated cardiomyopathy caused by mutation in TTN, cardiomyopathy, dilated, 1G

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

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Familial isolated dilated cardiomyopathy (11) ↑ Autosomal dominant titinopathy (0)

Including sub-types (12) Tagged with Dilated cardiomyopathy 1G (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.