Wilson disease (Q40119): Difference between revisions

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Latest revision as of 05:48, 13 August 2026

Wilson disease is an autosomal recessive disorder of copper metabolism characterised by the toxic accumulation of copper, mainly in the liver and central nervous system that may present as hepatic, neurologic or psychiatric forms.

Language	Label	Description	Also known as
default for all languages	5C64.00
English	Wilson disease	Wilson disease is an autosomal recessive disorder of copper metabolism characterised by the toxic accumulation of copper, mainly in the liver and central nervous system that may present as hepatic, neurologic or psychiatric forms.