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| Genomic newborn screening: BabyScreen+ v2.0 | UGT1A4 | Gene migrated from ENSG00000244474 to ENSG00000244474 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | UGT1A4 |
Zornitza Stark gene: UGT1A4 was added gene: UGT1A4 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene 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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