Catalog
Familial-genetic hypertrophic cardiomyopathy
Link to WHO Definition
Familial-genetic hypertrophic cardiomyopathy – http://id.who.int/icd/entity/1408928442
Familial isolated hypertrophic cardiomyopathy is the presence of non-syndromic hypertrophic cardiomyopathy in multiple members of a pedigree, or in the presence of a genetic mutation known to be significantly associated with hypertrophic cardiomyopathy.
Parents
Children
- Hypertrophic cardiomyopathy due to glycogen storage disease
- Hypertrophic cardiomyopathy due to lysosomal storage disease
- Sarcomeric hypertrophic cardiomyopathy
- Syndromic hypertrophic cardiomyopathy
- Hypertrophic cardiomyopathy due to mitochondrial disorder
- Other specified familial diseases associated with hypertrophic cardiomyopathy
- Hypertrophic cardiomyopathy due to disorder of fatty acid metabolism
- Hypertrophic cardiomyopathy due to primary amyloidosis