Gilbert syndrome (Q40114): Difference between revisions
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A síndrome de Gilbert é uma doença hereditária do fígado caracterizada por icterícia devido à hiperbilirrubinemia não conjugada, resultante de uma deficiência parcial na atividade da bilirrubina glucuronosiltransferase hepática. | |||
| description / en | description / en | ||
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. | |||
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. |
