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Disease Ontology Browser
Wilson disease (DOID:893)
Alliance: disease page
Synonyms: Cerebral pseudosclerosis; hepatolenticular degeneration; Westphal pseudosclerosis; Westphal-Strumpell syndrome; Wilson's disease
Alt IDs: OMIM:277900, ICD10CM:E83.01, MESH:D006527, NCI:C84756, UMLS_CUI:C0019202
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.

Disease References using Mouse Models (7)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory