Familial dilated cardiomyopathy with conduction defect due to LMNA mutation - CISMeF

" /> Familial dilated cardiomyopathy with conduction defect due to LMNA mutation - CISMeF

CISMeF

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Familial dilated cardiomyopathy with conduction defect due to LMNA mutationICD-11 More detail

Preferred Label : Familial dilated cardiomyopathy with conduction defect due to LMNA mutation;

Details

Origin ID

1141396375;

Currated CISMeF NLP mapping
- Cardiomyopathy, dilated, 1a [OMIM Phenotype]
- Familial dilated cardiomyopathy with conduction defect due to LMNA mutation [ORDO Disease]
- Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) [SNOMED CT concept]
- dilated cardiomyopathy 1A [DO Concept]

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06/05/2025

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