Disease
|
Abbr
|
Host
|
Etiology
|
Animal Prion Diseases
|
scrapie
|
—
|
sheep and goats
|
unknown origin
|
transmissible mink encephalopathy
|
TME
|
mink
|
sheep or cattle origin
|
chronic wasting disease
|
CWD
|
cervids
|
unknown origin
|
bovine spongiform encephalopathy
|
BSE
|
cattle
|
unknown origin
|
exotic ungulate spongiform encephalopathy
|
EUE
|
Nyala, Kudu
|
BSE origin
|
feline spongiform encephalopathy
|
FSE
|
cats
|
BSE origin
|
non-human primate spongiform encephalopathy
|
NHP
|
lemurs
|
BSE origin
|
Human Prion Diseases
|
Kuru
|
—
|
human
|
ritualistic cannibalism
|
sporadic Creutzfeld-Jakob disease
|
sCJD
|
human
|
spontaneous mutation of PrPC to PrPSc
|
familial Creutzfeld-Jakob disease
|
fCJD
|
human
|
mutations in PRNP gene
|
Gerstmann-Straüssler-Scheinker syndrome
|
GSS
|
human
|
mutations in PRNP gene
|
iatrogenic Creutzfeld-Jakob disease
|
iCJD
|
human
|
infection from surgical exposure to sCJD
|
fatal familial insomnia
|
FFI
|
human
|
PRNP haplotype 178N-129M
|
variant Creutzfeld-Jakob disease
|
vCJD
|
human
|
BSE origin
|
sporadic fatal insomnia
|
sFI
|
human
|
spontaneous mutation of PrPC to PrPSc
|
variably protease-sensitive prionopathy
|
VPSPr
|
human
|
spontaneous mutation of PrPC to PrPSc
|