Crigler-Najjar syndrome type 1 (Q91602): Difference between revisions
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13 August 2026
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Latest revision as of 18:38, 15 August 2026
Crigler-Najjar syndrome type 1 is the most severe form of Crigler-Najjar syndrome, a hereditary disorder of hepatic bilirubin conjugation, characterised by severe neonatal unconjugated hyperbilirubinemia due to a complete absence of hepatic bilirubin glucuronosyltransferase (BGT).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1098453659 |
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| English | Crigler-Najjar syndrome type 1 |
Crigler-Najjar syndrome type 1 is the most severe form of Crigler-Najjar syndrome, a hereditary disorder of hepatic bilirubin conjugation, characterised by severe neonatal unconjugated hyperbilirubinemia due to a complete absence of hepatic bilirubin glucuronosyltransferase (BGT). |
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CID11:ID_1098453659
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dki-india-ID_1098453659
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Concluído
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13 August 2026
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