has material basis in germline mutation in JPH2 cardiomyopathy, dilated, 2E https://github.com/monarch-initiative/mondo/issues/7693 https://www.malacards.org/card/cardiomyopathy_dilated_2e MONDO:0030366 CMD2E OMIM:619492 MEDGEN:1794180 DOID:0081161 GARD:0025554 A dilated cardiomyopathy that is characterized by neonatal or early childhood onset of dilated cardiomyopathy, with rapid progression to cardiac failure and death unless patients undergo cardiac transplantation and that has material basis in homozygous or compound heterozygous mutation in the JPH2 gene on chromosome 20q13. cardiomyopathy, dilated, 2E UMLS:C5561970 familial isolated dilated cardiomyopathy