Catalog
Familial-genetic dilated cardiomyopathy
Link to WHO Definition
Familial-genetic dilated cardiomyopathy – http://id.who.int/icd/entity/423719003
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)
Parents
Children
- Dilated cardiomyopathy due to fatty acid oxidation disorder
- Dilated cardiomyopathy due to mitochondrial myopathy
- Dilated cardiomyopathy due to neuromuscular disease
- Dilated cardiomyopathy due to glycogen branching enzyme deficiency
- Dilated cardiomyopathy due to lysosomal storage disorder
- X-linked infantile dilated cardiomyopathy
- Sarcomeric dilated cardiomyopathy
- Familial isolated dilated cardiomyopathy