has material basis in germline mutation in RPL3L cardiomyopathy, dilated, 2D https://github.com/monarch-initiative/mondo/issues/7693 https://www.malacards.org/card/cardiomyopathy_dilated_2d CMD2D 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. MEDGEN:1782612 DOID:0081160 OMIM:619371 GARD:0025531 cardiomyopathy, dilated, 2D UMLS:C5543535 familial isolated dilated cardiomyopathy