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Concept information

Preferred term

prion diseases

Type

  • Topic

Definition

  • Information 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.

Synonyms

  • spongiform encephalopathies
  • subacute spongiform encephalopathy
  • subacute transmissible spongiform encephalopathies
  • transmissible spongiform encephalopathies
  • TSE (transmissible spongiform encephalopathies)

In other languages

URI

https://lod.nal.usda.gov/nalt/18995

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RDF/XML TURTLE JSON-LD Created 1/19/06, last modified 2/25/16