DISEASES

Disease-gene associations mined from literature

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Human genes for Wernicke-Korsakoff syndrome

Wernicke-Korsakoff syndrome [DOID:10915]

A nutritional deficiency disease that is characterized by ophthalmoplegia, ataxia, change in mental status and acute onset of severe memory impairment without any dysfunction in intellectual abilities, and has_material_basis_in thiamine deficiency.

Synonyms:  Wernicke-Korsakoff syndrome,  DOID:10915,  WernickeKorsakoff syndrome,  Wernicke-Korsakoff disease,  Wernicke-Korsakoff disorder ...

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.