familial encephalopathy with neuroserpin inclusion bodies

Preferred Label : familial encephalopathy with neuroserpin inclusion bodies;

MeSH synonym : encephalopathy, familial, with collins bodies; encephalopathy, familial, with neuroserpin inclusion bodies; familial dementia with neuroserpin inclusion bodies; FENIB familiar encephalopathy with neuroserpin inclusion bodies;

Détails

Origin ID

C536841;

UMLS CUI

C1858680;

Automatic exact mappings (from CISMeF team)
- Familial encephalopathy with neuroserpin inclusion bodies [ICD-11 More detail]
CISMeF manual mappings
- Familial encephalopathy with neuroserpin inclusion bodies [ORDO Disease]
Currated CISMeF NLP mapping
- Encephalopathy, familial, with neuroserpin inclusion bodies [OMIM Phenotype]
- Familial encephalopathy with neuroserpin inclusion bodies (disorder) [SNOMED CT concept]
- familial encephalopathy with neuroserpin inclusion bodies [DO Concept]
DO Cross reference
- familial encephalopathy with neuroserpin inclusion bodies [DO Concept]
MeSH term(s) associated for indexing
- epilepsies, myoclonic [MeSH Descriptor]
- heredodegenerative disorders, nervous system [MeSH Descriptor]
ORDO relation(s)
- Familial encephalopathy with neuroserpin inclusion bodies [ORDO Disease]
Record concept(s)
- Familial encephalopathy with neuroserpin inclusion bodies [MeSH 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]

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