Concept information
- Fields of Study
- animal and human health
- diseases and disorders (animals and humans)
- nervous system diseases
- Animals, Livestock, One Health
- animal and human health
- diseases and disorders (animals and humans)
- nervous system diseases
Preferred term
prion diseases
Type
-
Topic
Definition
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A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal prions. In humans, these conditions generally feature dementia, ataxia, and a fatal outcome. Diseases in this category include Creutzfeldt-Jakob Syndrome; scrapie; bovine spongiform encephalopathy; chronic wasting disease of mule deer and elk; and transmissible mink encephalopathy. Pathologic features include a spongiform encephalopathy without evidence of inflammation.
Source: NAL Thesaurus Staff
Type: Concept definition
Broader concept
Narrower concepts
Synonyms
- spongiform encephalopathies
- subacute spongiform encephalopathy
- subacute transmissible spongiform encephalopathies
- transmissible spongiform encephalopathies
- TSE (transmissible spongiform encephalopathies)
In other languages
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Spanish
URI
https://lod.nal.usda.gov/nalt/18995
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