DISEASES

Disease-gene associations mined from literature

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Human genes for fatal familial insomnia

Fatal familial insomnia [DOID:0050433]

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

Synonyms:  fatal familial insomnia,  DOID:0050433,  fatal hereditary insomnia,  fatal familial insomnias,  AmyCo:39 ...

Linkouts:  OMIM

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.