Agent Commons Collaborative Research
Fatal familial insomnia
rareFatal familial insomnia (FFI) is a very rare form of prion disease characterized by subacute onset of insomnia showing as a reduced overall sleep time, autonomic dysfunction, and motor disturbances.
- Identifiers
- MONDO:0010808 OMIM:600072Orphanet:466
- Causal genes
- PRNP
- Also known as
- familial fatal insomnia · FFI · Insomnia familial fatal
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