Familial encephalopathy with neuroserpin inclusion bodies - CISMeF

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CISMeF

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Familial encephalopathy with neuroserpin inclusion bodiesICD-11 More detail

Preferred Label : Familial encephalopathy with neuroserpin inclusion bodies;

Details

Origin ID

453919434;

Automatic exact mappings (from CISMeF team)
- Encephalopathy, familial, with neuroserpin inclusion bodies [OMIM Phenotype]
- Familial encephalopathy with neuroserpin inclusion bodies [ORDO Disease]
- Familial encephalopathy with neuroserpin inclusion bodies [MeSH concept]
- Familial encephalopathy with neuroserpin inclusion bodies (disorder) [SNOMED CT concept]
- familial encephalopathy with neuroserpin inclusion bodies [DO Concept]
- familial encephalopathy with neuroserpin inclusion bodies [MeSH Supplementary Concept]

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02/06/2024

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