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fatal familial insomnia

Disease Summary
Associated Targets (2)
Tchem

1

Tbio

1


GARD Rare
Mondo Description Fatal 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.
Uniprot Description Autosomal dominant disorder and is characterized by neuronal degeneration limited to selected thalamic nuclei and progressive insomnia.
Disease Ontology Description A prion disease that is characterized by insomnia, hallucinations, dementia and death, located_in the brain.
Mondo Term and Equivalent IDs
MONDO:0010808:  fatal familial insomnia
GARD:0006429: 
ICD10:A81.83: 
MESH:D034062: 
NCIT:C84711: 
Orphanet:466: 
SCTID:83157008: 
UMLS:C0206042: