Crigler-Najjar syndrome type 1 (Q91602): Difference between revisions

@@ description / pt-br / description / pt-br @@
+A síndrome de Crigler-Najjar tipo 1 é a forma mais grave da síndrome de Crigler-Najjar, um distúrbio hereditário da conjugação da bilirrubina hepática, caracterizado por hiperbilirrubinemia neonatal não conjugada grave devido à ausência completa de bilirrubina hepática glucuronosiltransferase.
@@ description / en / description / en @@
+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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+https://id.who.int/icd/entity/1098453659
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+CID11:ID_1098453659
@@ Property / CURIE: CID11:ID_1098453659 / rank @@
+Normal rank
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@@ Property / Canary Token: dki-india-ID_1098453659 / rank @@
+Normal rank
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+Concluído
@@ Property / Verification Status: Concluído / rank @@
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@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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After 0
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++2026-08-13T00:00:00Z
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++00:00
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 After
@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank

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
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).