dilated cardiomyopathy 2E (DOID:0081161)
Alliance: disease page
Alt IDs: OMIM:619492
Definition: A dilated cardiomyopathy that is characterized by neonatal or early childhood onset of dilated cardiomyopathy, with rapid progression to cardiac failure and death unless patients undergo cardiac transplantation and that has_material_basis_in homozygous or compound heterozygous mutation in the JPH2 gene on chromosome 20q13.