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| Likely inborn error of metabolism - targeted testing not possible v1.47 | UGT1A1 |
Ivone Leong Source NHS GMS was added to UGT1A1. Source London North GLH was added to UGT1A1. |
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| Likely inborn error of metabolism - targeted testing not possible v0.4 | UGT1A1 |
Ellen McDonagh gene: UGT1A1 was added gene: UGT1A1 was added to Inborn errors of metabolism. Sources: Expert Review Green Mode of inheritance for gene: UGT1A1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: UGT1A1 were set to 27604308; 24816252 Phenotypes for gene: UGT1A1 were set to Crigler-Najjar syndrome, type I 218800; Bilirubin UDP-glucuronosyltransferase 1 deficiency (Disorders of bile acid metabolism and transport); Crigler-Najjar syndrome, type II 606785 |
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