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

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)