Gilbert syndrome (Q40114): Difference between revisions
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13 August 2026
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Latest revision as of 05:47, 13 August 2026
Gilbert's syndrome is an inherited liver disorder characterised by jaundice due to unconjugated hyperbilirubinemia, resulting from a partial deficiency in hepatic bilirubin glucuronosyltransferase activity.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C58.01 |
||
| English | Gilbert syndrome |
Gilbert's syndrome is an inherited liver disorder characterised by jaundice due to unconjugated hyperbilirubinemia, resulting from a partial deficiency in hepatic bilirubin glucuronosyltransferase activity. |
Statements
CID11:5C58.01
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dki-india-5C58.01
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Concluído
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13 August 2026
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