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Infections > Central Nervous System Infections > Prion Diseases
Nervous System Diseases > Central Nervous System Diseases > Central Nervous System Infections > Prion Diseases
Nervous System Diseases > Neurodegenerative Diseases > Prion Diseases

Käytettävä termi

Prion Diseases  

Tyyppi

  • Topical Descriptor

Yläkäsite

Alakäsitteet

Assosiatiiviset käsitteet

Ohjaustermit

  • Dementias, Transmissible
  • Dementia, Transmissible
  • Disorder, Prion-Induced
  • Disorders, Prion-Induced
  • Encephalopathies, Spongiform, Transmissible
  • Encephalopathies, Transmissible Spongiform
  • Encephalopathy, Transmissible Spongiform
  • Prion-Associated Disorders
  • Prion Disease
  • Prion Induced Disorder
  • Prion-Induced Disorder
  • Prion-Induced Disorders
  • Prion Protein Disease
  • Prion Protein Diseases
  • Spongiform Encephalopathies, Transmissible
  • Spongiform Encephalopathy, Transmissible
  • Transmissible Dementia
  • Transmissible Dementias
  • Transmissible Spongiform Encephalopathies
  • Transmissible Spongiform Encephalopathy

Huomautus

  • general or unspecified; prefer specifics

Käyttöhuomautus

  • A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83)

Huomautus muutoshistoriasta

  • 1993

Muunkieliset termit

URI

http://www.yso.fi/onto/mesh/D017096

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RDF/XML TURTLE JSON-LD Luotu 22.5.1992, viimeksi muokattu 11.4.2022