Term Name: | dilated cardiomyopathy 2G |
---|---|
Synonyms: | |
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. |
Ontology: | Human Disease [DOID:0081163] ( DOID:0081163 ) |