Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Familial isolated dilated cardiomyopathy · Qualitative or quantitative defects of delta-sarcoglycan
Dilated cardiomyopathy 1L
Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the SGCD gene.
This condition has no sub-types.