Agent Commons Collaborative Research

Prion disease

rare

A 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
Disease Subtypes
Creutzfeldt Jacob disease 5
Gerstmann-Straussler-Scheinker syndrome
Huntington disease-like 1
PrP systemic amyloidosis
Familial Alzheimer-like prion disease
Fatal familial insomnia
Kuru
Scrapie
Spongiform encephalopathy with neuropsychiatric features
Sporadic fatal insomnia

Rare disease

Projects

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