has material basis in germline mutation in LMOD2 cardiomyopathy, dilated, 2G https://github.com/monarch-initiative/mondo/issues/7693 https://www.malacards.org/card/cardiomyopathy_dilated_2g DOID:0081163 UMLS:C5676995 CMD2G GARD:0025652 A dilated cardiomyopathy that is characterized by early-onset severe dilated cardiomyopathy that progresses rapidly to heart failure in the neonatal period without evidence of intervening hypertrophy and that has material basis in homozygous or compound heterozygous mutation in the LMOD2 gene on chromosome 7q31. OMIM:619897 MONDO:0030887 MEDGEN:1801983 cardiomyopathy, dilated, 2G familial isolated dilated cardiomyopathy