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Name: Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder) See more descriptions.

- Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation
- Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
- Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder)
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Concept ID: 766883006
Read Codes:
ICD-10 Codes: I420
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