Wilson disease (Q40119)
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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. |
Statements
CID11:5C64.00
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dki-india-5C64.00
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Concluído
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13 August 2026
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