MeSH Browser

MeSH Supplementary: Familial encephalopathy with neuroserpin inclusion bodies
Unique ID: C536841
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536841
Entry Term(s): Encephalopathy, Familial, With Neuroserpin Inclusion Bodies; Encephalopathy, familial, with Collins bodies; FENIB familiar encephalopathy with neuroserpin inclusion bodies; Familial Dementia with Neuroserpin Inclusion Bodies
Registry Numbers: 0
Heading Mapped to: *Epilepsies, Myoclonic; *Heredodegenerative Disorders, Nervous System
Frequency: 16
Date of Entry: 2010/08/25
Revision Date: 2023/08/10

Familial encephalopathy with neuroserpin inclusion bodies MeSH Supplementary Concept Data 2025