Defective UGT1A4 causes hyperbilirubinemia - Wikidata - wikimedia - TriplyDB

Defective UGT1A4 causes hyperbilirubinemia

Defective UGT1A4 causes hyperbilirubinemia

http://www.wikidata.org/entity/Q45316498

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Defective UGT1A4 does not transfer GlcA from UDP-GlcA to BIL Defective UGT1A4 does not transfer GlcA from UDP-GlcA to BMG

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Metabolic disorders of biological oxidation enzymes

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Defective UGT1A4 causes hyperbilirubinemia

http://www.wikidata.org/entity/Q45316498

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An instance of the biological ...... rbilirubinemia in Homo sapiens

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Defective UGT1A4 causes hyperbilirubinemia

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label

Defective UGT1A4 causes hyperbilirubinemia

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Defective UGT1A4 causes hyperbilirubinemia

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New insights in bilirubin metabolism and their clinical implications

Hyperbilirubinemia syndromes (Gilbert-Meulengracht, Crigler-Najjar, Dubin-Johnson, and Rotor syndrome)

Hematologically important mutations: bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler-Najjar syndromes.

Influence of mutations associated with Gilbert and Crigler-Najjar type II syndromes on the glucuronidation kinetics of bilirubin and other UDP-glucuronosyltransferase 1A substrates.

Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate- glucuronosyltransferase gene.

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reactome:R-HSA-5579016

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biological pathway

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Metabolic disorders of biological oxidation enzymes

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R-HSA-5579016

http://www.w3.org/2001/XMLSchema#string

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Defective UGT1A4 does not transfer GlcA from UDP-GlcA to BIL

Defective UGT1A4 does not transfer GlcA from UDP-GlcA to BMG

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