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Summary Literature (0)
DOID:0050433 - fatal familial insomnia


Disease Ontology Definition:A prion disease that is characterized by insomnia, hallucinations, dementia and death, located_in the brain.

Synonyms:

Xenbase Genes : prnp

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010808 - fatal familial insomnia

OMIM:
OMIM:600072 - FATAL FAMILIAL INSOMNIA; FFI

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): prion disease (is_a)