BC43.00
Familial-genetic dilated cardiomyopathy
Cardiomiopatia dilatada genética familiar
CategoryDefinition
Familial-genetic dilated cardiomyopathy is the presence of dilated cardiomyopathy that is present in multiple members of a pedigree, or in the presence of a genetic mutation known to be significantly associated with dilated cardiomyopathy. Additional information: Candidate cytoskeletal and Z disk–encoding genes, most of whom are hypothesized to lead to abnormalities in force transmission, include δ-sarcoglycan, β-sarcoglycan, desmin, lamin A/C, metavinculin, muscle LIM protein, titin, α-actinin-2, nebulette, myopalladin, and ZASP (Z band alternatively spliced PDZ domain protein)
Index Terms
Familial-genetic dilated cardiomyopathyfamilial dilated cardiomyopathyprimary familial dilated cardiomyopathyfamilial congestive cardiomyopathyFamilial isolated dilated cardiomyopathyDilated cardiomyopathy due to fatty acid oxidation disorderFatty acid oxidation or ketogenesis disorder with dilated cardiomyopathyDilated cardiomyopathy due to primary carnitine deficiencyDilated-hypokinetic cardiomyopathy due to primary carnitine deficiencyDilated cardiomyopathy due to malonyl-CoA decarboxylase deficiencydilated cardiomyopathy due to malonic aciduriaDilated-hypokinetic cardiomyopathy due to malonyl-CoA decarboxylase deficiencyDilated cardiomyopathy due to mitochondrial myopathymitochondrial disease with dilated cardiomyopathyMitochondrial dilated cardiomyopathyHistiocytoid cardiomyopathyfocal lipid cardiomyopathyinfantile xanthomatous cardiomyopathyoncocytic cardiomyopathyDilated cardiomyopathy due to Cytochrome C oxidase deficiencyDilated cardiomyopathy due to Barth syndromeDilated cardiomyopathy due to Kearns–Sayre syndromeDilated cardiomyopathy due to MELASDilated cardiomyopathy due to MELAS - [Mitochondrial Encephalopathy, Lactic acidosis and Stroke-like episodes]Dilated cardiomyopathy due to MERRFDilated cardiomyopathy due to MERRF - [myoclonic epilepsy with ragged-red fibers]Dilated cardiomyopathy due to neuromuscular diseaseNeuromuscular disease with dilated cardiomyopathyDilated cardiomyopathy due to dystrophinopathyDilated cardiomyopathy due to Duchenne muscular dystrophyDilated cardiomyopathy due to Becker muscular dystrophyDilated cardiomyopathy due to laminopathyDilated cardiomyopathy due to laminopathy [LMNA]Dilated cardiomyopathy due to lamin A/C mutationFamilial dilated cardiomyopathy with conduction defect due to LMNA mutationDilated cardiomyopathy due to Emery-Dreifus muscular dystrophyDilated cardiomyopathy due to limb-girdle muscular dystrophyDilated cardiomyopathy due to congenital muscular dystrophyDilated cardiomyopathy due to spinal muscular atrophyDilated cardiomyopathy due to SMA - [spinal muscular atrophy]Dilated cardiomyopathy due to polymyositisSarcomeric dilated cardiomyopathyX-linked infantile dilated cardiomyopathyDilated cardiomyopathy due to lysosomal storage disorderdilated-hypokinetic cardiomyopathy due to lysosomal storage disorderDilated cardiomyopathy due to mucopolysaccharidosesdilated-hypokinetic cardiomyopathy due to mucopolysaccharidosesDilated cardiomyopathy due to sphingolipidosesdilated-hypokinetic cardiomyopathy due to sphingolipidosesDilated cardiomyopathy due to Gaucher disease