Prion diseases
URI(s)
- http://id.loc.gov/authorities/subjects/sh92003842
- info:lc/authorities/sh92003842
- http://id.loc.gov/authorities/sh92003842#concept
Instance Of
Scheme Membership(s)
Collection Membership(s)
Variants
- Encephalopathies, Spongiform
- Prion infections
- Spongiform encephalopathies
- Transmissible spongiform encephalopathies
- Unconventional slow virus diseases
Broader Terms
Narrower Terms
Related Terms
Exact Matching Concepts from Other Schemes
Closely Matching Concepts from Other Schemes
Sources
- found: Work cat.: 92-1704: Prion diseases of humans and animals, 1992.
- found: Dulbecco. Virology, 1988:pp. 16-17, 142-145, table 51-4.
- found: Cecil textbook of medicine, 1992.
- found: MESH(Prion diseases x Encephalopathies, Spongiform; Spongiform encephalopathies; Transmissible. SN: Transmissible and genetic neurodegenerative diseases of humans and animals caused by prions. The literature has sometimes referred to these as unconventional slow virus diseases.)
LC Classification
- QR201.P737
- RA644.P93
Change Notes
- 1992-07-16: new
- 1997-03-18: revised
Alternate Formats
