fatal familial insomnia

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: prnp

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010808 - fatal familial insomnia

MONDO:0010808 - fatal familial insomnia

MIM:

MIM:600072 - FATAL FAMILIAL INSOMNIA; FFI

MIM:600072 - FATAL FAMILIAL INSOMNIA; FFI

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): prion disease (is_a)