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Metadata
ID	DOID:0081163
Name	dilated cardiomyopathy 2G
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. https://pubmed.ncbi.nlm.nih.gov/31517052/
Xrefs	MIM:619897
Parent Relationships	is_a dilated cardiomyopathy is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance