Hypertrophic cardiomyopathy 9

MONDO:0013412

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

Also known as: CMH9, TTN hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, 9, cardiomyopathy, familial hypertrophic, type 9, hypertrophic cardiomyopathy caused by mutation in TTN, hypertrophic cardiomyopathy type 9

12 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 9 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Familial hypertrophic cardiomyopathy (86) ↑ Autosomal dominant titinopathy (0)

Including sub-types (12) Tagged with Hypertrophic cardiomyopathy 9 (0)

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