DOID:2384 - Wernicke encephalopathy
Disease Ontology Definition:A brain disease that is characterised by the presence of neurological symptoms of ophthalmoplegia, ataxia, and confusion caused by biochemical lesions of the central nervous system after exhaustion of B-vitamin reserves, in particular thiamine (vitamin B1).
Synonyms: Wernicke's disease, Wernicke's encephalopathy
|MONDO:0007020 - Wernicke encephalopathy|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): brain disease (is_a)