Familial encephalopathy with neuroserpin inclusion bodies

Preferred Label : Familial encephalopathy with neuroserpin inclusion bodies;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0531302;

UMLS CUI

C1858680;

Automatic exact mappings (from CISMeF team)
- Familial encephalopathy with neuroserpin inclusion bodies [ICD-11 More detail]
Currated CISMeF NLP mapping
- Encephalopathy, familial, with neuroserpin inclusion bodies [OMIM Phenotype]
- Familial encephalopathy with neuroserpin inclusion bodies [ORDO Disease]
- Familial encephalopathy with neuroserpin inclusion bodies (disorder) [SNOMED CT concept]
- familial encephalopathy with neuroserpin inclusion bodies [DO Concept]
Related record
- familial encephalopathy with neuroserpin inclusion bodies [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Encephalopathy, familial, with neuroserpin inclusion bodies [OMIM Phenotype]
- Familial encephalopathy with neuroserpin inclusion bodies [ORDO Disease]
- Familial encephalopathy with neuroserpin inclusion bodies (disorder) [SNOMED CT concept]
- familial encephalopathy with neuroserpin inclusion bodies [DO Concept]