Visningssätt för begreppens/termernas förhållanden:
Det sätt begreppsrelationer visas:
Det sätt begreppsrelationer visas:
Prionsjukdomar
Hierarki: | ∟ ∟ ∟ Prionsjukdomar 24 sidobegrepp7 underordnad begrepp∟ ∟ ∟ ∟ Prionsjukdomar 24 sidobegrepp7 underordnad begrepp∟ ∟ ∟ Prionsjukdomar 24 sidobegrepp7 underordnad begreppX |
Bredare villkor: | |
Snävare villkor: | |
Anmärkning: | Slow Virus Diseases (1966-1992)X |
Anmärkning: | 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)
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Annotation: | GEN or unspecified: prefer specifics
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historyNote*: | 1993
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publicMeSHNote*: | 1993
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activeMeSHYear*: | |
dateCreated*: | 1992-05-22X |
dateEstablished*: | 1993-01-01X |
dateRevised*: | 2005-07-13X |
recordAuthorizer*: | agsX |
recordMaintainer*: | agsX |
recordOriginator*: | AGSX |
Typ: | |
Samordna villkor: | |
URI: | |
Termer och motsvarande begrepp: | Prionisairaudet (fi) XPrionitaudit (fi, ersatt) Prion Diseases (en) Transmissible Dementias (en, ersatt) Transmissible Spongiform Encephalopathies (en, ersatt) Spongiform Encephalopathies, Transmissible (en, ersatt) Prion-Induced Disorder (en, ersatt) Encephalopathies, Spongiform, Transmissible (en, ersatt) Inherited Human Transmissible Spongiform Encephalopathies (en, ersatt) Prion Protein Diseases (en, ersatt) Dementias, Transmissible (en, ersatt) |
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