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Disease Ontology Browser
fatal familial insomnia (DOID:0050433)
Alliance: disease page
Alt IDs: OMIM:600072, ICD10CM:A81.83, ICD9CM:046.72, MESH:D034062, NCI:C84711, UMLS_CUI:C0206042
Definition: A prion disease that is characterized by insomnia, hallucinations, dementia and death, located_in the brain.

Disease References using Mouse Models (2)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory