Familial-genetic hypertrophic cardiomyopathy

ICD-11 code : BC43.10;

Preferred Label : Familial-genetic hypertrophic cardiomyopathy;

ICD-11 definition : 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.;

ICD-11 synonym : Familial hypertrophic cardiomyopathy;

Details

Origin ID

1408928442;

Currated CISMeF NLP mapping
- Cardiomyopathy, familial hypertrophic [OMIM phenotypic series]
- Familial Hypertrophic Cardiomyopathy [NCIt concept]
- Primary familial hypertrophic cardiomyopathy (disorder) [SNOMED CT concept]
- Rare familial disorder with hypertrophic cardiomyopathy [ORDO Disease]
- cardiomyopathy, hypertrophic, familial [MeSH concept]
- cardiomyopathy, hypertrophic, familial [MeSH Descriptor]
- familial hypertrophic cardiomyopathy [DO Concept]
- familial hypertrophic cardiomyopathy [Disease (Nov.)]
- hypertrophic cardiomyopathy [DO Concept]
- primary familial hypertrophic cardiomyopathy [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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