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| Additional findings_Paediatric v1.0 | UGT1A4 | Gene migrated from ENSG00000244474 to ENSG00000244474 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | UGT1A4 |
Zornitza Stark gene: UGT1A4 was added gene: UGT1A4 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red Mode of inheritance for gene: UGT1A4 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: UGT1A4 were set to Crigler-Najjar syndrome |
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