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BC43.00 Familial-genetic dilated cardiomyopathy

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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)

code elsewhere

• Dilated cardiomyopathy due to glycogen branching enzyme deficiency  (5C51.3)

synonyms

• Familial-genetic dilated cardiomyopathy
• familial dilated cardiomyopathy
• primary familial dilated cardiomyopathy
• familial congestive cardiomyopathy
• Familial isolated dilated cardiomyopathy
• Dilated cardiomyopathy due to fatty acid oxidation disorder
• Fatty acid oxidation or ketogenesis disorder with dilated cardiomyopathy
• Dilated cardiomyopathy due to primary carnitine deficiency
• Dilated-hypokinetic cardiomyopathy due to primary carnitine deficiency
• Dilated cardiomyopathy due to malonyl-CoA decarboxylase deficiency
• dilated cardiomyopathy due to malonic aciduria
• Dilated-hypokinetic cardiomyopathy due to malonyl-CoA decarboxylase deficiency
• Dilated cardiomyopathy due to mitochondrial myopathy
• mitochondrial disease with dilated cardiomyopathy
• Mitochondrial dilated cardiomyopathy
• Histiocytoid cardiomyopathy
• focal lipid cardiomyopathy
• infantile xanthomatous cardiomyopathy
• oncocytic cardiomyopathy
• Dilated cardiomyopathy due to Cytochrome C oxidase deficiency
• Dilated cardiomyopathy due to Barth syndrome
• Dilated cardiomyopathy due to Kearns–Sayre syndrome
• Dilated cardiomyopathy due to MELAS
• Dilated cardiomyopathy due to MELAS - [Mitochondrial Encephalopathy, Lactic acidosis and Stroke-like episodes]
• Dilated cardiomyopathy due to MERRF
• Dilated cardiomyopathy due to MERRF - [myoclonic epilepsy with ragged-red fibers]
• Dilated cardiomyopathy due to neuromuscular disease
• Neuromuscular disease with dilated cardiomyopathy
• Dilated cardiomyopathy due to dystrophinopathy
• Dilated cardiomyopathy due to Duchenne muscular dystrophy
• Dilated cardiomyopathy due to Becker muscular dystrophy
• Dilated cardiomyopathy due to laminopathy
• Dilated cardiomyopathy due to laminopathy [LMNA]
• Dilated cardiomyopathy due to lamin A/C mutation
• Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
• Dilated cardiomyopathy due to Emery-Dreifus muscular dystrophy
• Dilated cardiomyopathy due to limb-girdle muscular dystrophy
• Dilated cardiomyopathy due to congenital muscular dystrophy
• Dilated cardiomyopathy due to spinal muscular atrophy
• Dilated cardiomyopathy due to SMA - [spinal muscular atrophy]
• Dilated cardiomyopathy due to polymyositis
• Sarcomeric dilated cardiomyopathy
• X-linked infantile dilated cardiomyopathy
• Dilated cardiomyopathy due to lysosomal storage disorder
• dilated-hypokinetic cardiomyopathy due to lysosomal storage disorder
• Dilated cardiomyopathy due to mucopolysaccharidoses
• dilated-hypokinetic cardiomyopathy due to mucopolysaccharidoses
• Dilated cardiomyopathy due to sphingolipidoses
• dilated-hypokinetic cardiomyopathy due to sphingolipidoses
• Dilated cardiomyopathy due to Gaucher disease

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