Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Familial hypertrophic cardiomyopathy · Familial isolated dilated cardiomyopathy · Left ventricular noncompaction
Dilated cardiomyopathy 1C
A dilated cardiomyopathy that has material basis in mutation in the LDB3 gene on chromosome 10q23.2.
This condition has no sub-types.