Congenital disorder of glycosylation with dilated cardiomyopathy
ORPHA:371176Dilated cardiomyopathy
ORPHA:217604Dilated cardiomyopathy with ataxia
ORPHA:66634Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
ORPHA:2229Early-onset myopathy with fatal cardiomyopathy
ORPHA:289377Familial dilated cardiomyopathy
ORPHA:217607Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
ORPHA:300751Familial isolated dilated cardiomyopathy
ORPHA:154Fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy
ORPHA:217616Glycogen storage disease with hypertrophic cardiomyopathy
ORPHA:217572Histiocytoid cardiomyopathy
ORPHA:137675Intermediate epidermolysis bullosa simplex with cardiomyopathy
ORPHA:508529Isolated atrial standstill
ORPHA:1344Kidney tubulopathy-dilated cardiomyopathy syndrome
ORPHA:73224Leigh syndrome with cardiomyopathy
ORPHA:70474Lysosomal disease with hypertrophic cardiomyopathy
ORPHA:217581Lysosomal disease with restrictive cardiomyopathy
ORPHA:217638Mitochondrial disease with dilated cardiomyopathy
ORPHA:217613Mitochondrial DNA-related cardiomyopathy and hearing loss
ORPHA:1349Neuromuscular disease with dilated cardiomyopathy
ORPHA:217610Non-familial dilated cardiomyopathy
ORPHA:217629Non-familial rare disease with dilated cardiomyopathy
ORPHA:324767Peripartum cardiomyopathy
ORPHA:563Rare cardiomyopathy
ORPHA:167848Sensorineural deafness with dilated cardiomyopathy
ORPHA:217622Severe dilated cardiomyopathy due to lamin A/C mutation
ORPHA:83618Syndrome associated with dilated cardiomyopathy
ORPHA:217619Syndrome associated with hypertrophic cardiomyopathy
ORPHA:217595Tako-Tsubo cardiomyopathy
ORPHA:66529Unclassified cardiomyopathy
ORPHA:217678