BC43.00
category
Familial-genetic dilated cardiomyopathy
Definition
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)
Also indexed as
Dilated cardiomyopathy due to Barth syndromeDilated cardiomyopathy due to Becker muscular dystrophyDilated cardiomyopathy due to Cytochrome C oxidase deficiencyDilated cardiomyopathy due to Duchenne muscular dystrophyDilated cardiomyopathy due to Emery-Dreifus muscular dystrophyDilated cardiomyopathy due to Gaucher diseaseDilated 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 SMA - [spinal muscular atrophy]Dilated cardiomyopathy due to congenital muscular dystrophyDilated cardiomyopathy due to dystrophinopathyDilated cardiomyopathy due to fatty acid oxidation disorderDilated cardiomyopathy due to lamin A/C mutationDilated cardiomyopathy due to laminopathyDilated cardiomyopathy due to laminopathy [LMNA]Dilated cardiomyopathy due to limb-girdle muscular dystrophyDilated cardiomyopathy due to lysosomal storage disorderDilated cardiomyopathy due to malonyl-CoA decarboxylase deficiencyDilated cardiomyopathy due to mitochondrial myopathyDilated cardiomyopathy due to mucopolysaccharidosesDilated cardiomyopathy due to neuromuscular diseaseDilated cardiomyopathy due to polymyositisDilated cardiomyopathy due to primary carnitine deficiencyDilated cardiomyopathy due to sphingolipidosesDilated cardiomyopathy due to spinal muscular atrophyDilated-hypokinetic cardiomyopathy due to malonyl-CoA decarboxylase deficiencyDilated-hypokinetic cardiomyopathy due to primary carnitine deficiencyFamilial dilated cardiomyopathy with conduction defect due to LMNA mutationFamilial isolated dilated cardiomyopathyFamilial-genetic dilated cardiomyopathyFatty acid oxidation or ketogenesis disorder with dilated cardiomyopathyHistiocytoid cardiomyopathyMitochondrial dilated cardiomyopathyNeuromuscular disease with dilated cardiomyopathySarcomeric dilated cardiomyopathyX-linked infantile dilated cardiomyopathydilated cardiomyopathy due to malonic aciduriadilated-hypokinetic cardiomyopathy due to lysosomal storage disorderdilated-hypokinetic cardiomyopathy due to mucopolysaccharidosesdilated-hypokinetic cardiomyopathy due to sphingolipidosesfamilial congestive cardiomyopathyfamilial dilated cardiomyopathyfocal lipid cardiomyopathyinfantile xanthomatous cardiomyopathymitochondrial disease with dilated cardiomyopathyoncocytic cardiomyopathyprimary familial dilated cardiomyopathy