Cardiomyopathy, dilated, 2D

MONDO:0030300

A dilated cardiomyopathy that is characterized by neonatal onset of severe cardiomyopathy, with rapid progression to cardiac decompensation and death unless the patient undergoes heart transplantation and that has material basis in homozygous or compound heterozygous mutation in the RPL3L gene on chromosome 16p13.

Also known as: CMD2D, cardiomyopathy, dilated, 2D

218 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by