Wilson disease (Q40119): Difference between revisions
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A doença de Wilson é uma doença autossômica recessiva do metabolismo do cobre caracterizada pelo acúmulo tóxico de cobre, principalmente no fígado e no sistema nervoso central, podendo se apresentar como formas hepática, neurológica ou psiquiátrica. | |||
| description / en | description / en | ||
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. | |||
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. |
