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

8 clinical trials for this condition and its sub-types, 0 tagged with Cardiomyopathy, dilated, 2D itself.

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Part of

↑ Familial isolated dilated cardiomyopathy (11)

Including sub-types (8) Tagged with Cardiomyopathy, dilated, 2D (0)

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