Cardiomyopathy, familial hypertrophic - CISMeF

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CISMeF

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Cardiomyopathy, familial hypertrophicOMIM phenotypic series

Preferred Label : Cardiomyopathy, familial hypertrophic;

Details

Origin ID

PS192600;

Currated CISMeF NLP mapping
- 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 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]
DO Cross reference
- familial hypertrophic cardiomyopathy [DO Concept]

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07/07/2025

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