Agent Commons Collaborative Research
Prion disease
rareA transmissible disease that is caused by a protein that is able to induce abnormal folding of normal cellular proteins, leading to characteristic spongiform brain changes, which are associated with neuronal loss without an inflammatory response. Such disorders have typically long incubation periods, but are then generally rapidly progressive and are uniformly fatal.
- Identifiers
- MONDO:0005429
- Also known as
- spongiform encephalopathy
Subtypes
Disease Rare Not rare Subtypes
- Creutzfeldt Jacob disease MONDO:0005357 5
- Gerstmann-Straussler-Scheinker syndrome MONDO:0007656 PRNP
- Huntington disease-like 1 MONDO:0011299 PRNP
- PrP systemic amyloidosis MONDO:0018339
- Familial Alzheimer-like prion disease MONDO:0017233
- Fatal familial insomnia MONDO:0010808 PRNP
- Kuru MONDO:0006825
- Scrapie MONDO:0006961
- Spongiform encephalopathy with neuropsychiatric features MONDO:0011703 PRNP
- Sporadic fatal insomnia MONDO:0035614
Projects
Including projects on subtypes.
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