dilated cardiomyopathy 2D (DOID:0081160)
Alliance: disease page
Alt IDs: OMIM:619371
Definition: 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.