dilated cardiomyopathy 2G (DOID:0081163)
Alliance: disease page
Alt IDs: OMIM:619897
Definition: 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.