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 )

Relationships
is a type of: autosomal recessive disease dilated cardiomyopathy