Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:893 - Wilson disease

Disease Ontology Definition:A metal metabolism disease that is characterized by excess copper stored in various body tissues, particularly the liver, brain, and corneas of the eyes.

Synonyms: Cerebral pseudosclerosis, Westphal pseudosclerosis, Westphal-Strumpell syndrome, Wilson's disease, hepatolenticular degeneration,

Xenbase Genes : atp7b

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010200 - Wilson disease


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): liver disease (is_a), metal metabolism disorder (is_a)