Wernicke-Korsakoff syndrome

Summary

DOID:10915 - Wernicke-Korsakoff syndrome

Disease Ontology Definition: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: Korsakoff's psychosis, Korsakoff's psychosis (disorder), Korsakoff's syndrome, Korsakoff Syndrome, Korsakov psychosis, Korsakov's psychosis

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

: tkt

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010198 - Wernicke-Korsakoff syndrome

MONDO:0010198 - Wernicke-Korsakoff syndrome

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

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

Parent(s): nutritional deficiency disease (is_a), thiamine deficiency disease (is_a)