primary familial hypertrophic cardiomyopathy - CISMeF

" /> primary familial hypertrophic cardiomyopathy - CISMeF

CISMeF

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Primary familial hypertrophic cardiomyopathySNOMED Notion

Preferred Label : primary familial hypertrophic cardiomyopathy;

Details

Origin ID

D3-23120;

UMLS CUI

C0949658;

Currated CISMeF NLP mapping
- Cardiomyopathy, familial hypertrophic [OMIM phenotypic series]
- Familial Hypertrophic Cardiomyopathy [NCIt concept]
- Familial-genetic hypertrophic cardiomyopathy [ICD-11 Sub-sub category]
- Primary familial hypertrophic cardiomyopathy (disorder) [SNOMED CT concept]
- Rare familial disorder with hypertrophic cardiomyopathy [ORDO Disease]
- cardiomyopathy, hypertrophic, familial [MeSH Descriptor]
- cardiomyopathy, hypertrophic, familial [MeSH concept]
- familial hypertrophic cardiomyopathy [DO Concept]
- familial hypertrophic cardiomyopathy [Disease (Nov.)]
- hypertrophic cardiomyopathy [DO Concept]
ICD-10 exact mapping(s)
- Other hypertrophic cardiomyopathy [ICD-10 Sub-category (who)]
Metaterm(s)
- cardiology [CISMeF Metaterm]
Référence SNOMED
- familial disease, nos [SNOMED Notion]
- heart, nos [SNOMED Notion]
- hypertrophy, nos [SNOMED Notion]
- left ventricle, nos [SNOMED Notion]
SNOMED CT concept
- Primary familial hypertrophic cardiomyopathy (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 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 Descriptor]
- cardiomyopathy, hypertrophic, familial [MeSH concept]
- familial hypertrophic cardiomyopathy [Disease (Nov.)]

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19/05/2024

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