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. [ Orphanet:466 ]

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:D034062 (Orphanet:466)
  • MedDRA:10072077 (Orphanet:466)
  • NCIT:C84711 (MONDO:equivalentTo)
  • ICD9:046.72 (DOID:0050433)
  • UMLS:C0206042 (Orphanet:466)
  • SCTID:83157008 (MONDO:equivalentTo)
  • OMIM:600072 (Orphanet:466)
  • ICD10:A81.8 (Orphanet:466)
  • DOID:0050433 (MONDO:equivalentTo)
  • Orphanet:466 (OMIM:600072)
  • ICD10:A81.83 (MONDO:equivalentTo)
  • GARD:0006429 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

definition

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.

exactMatch

http://identifiers.org/meddra/10072077

http://identifiers.org/omim/600072

http://www.orpha.net/ORDO/Orphanet_466

http://purl.obolibrary.org/obo/DOID_0050433

http://linkedlifedata.com/resource/umls/id/C0206042

http://identifiers.org/snomedct/83157008

http://purl.obolibrary.org/obo/NCIT_C84711

http://identifiers.org/mesh/D034062

has exact synonym

fatal familial insomnia

has related synonym

Insomnia, fatal familial

familial fatal insomnia

Insomnia familial fatal

FFI

fatal familial INSOMNIA

id

MONDO:0010808

seeAlso

https://rarediseases.info.nih.gov/diseases/6429/fatal-familial-insomnia