Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
BabyScreen+ newborn screening v0.0 | UGT1A5 |
Zornitza Stark gene: UGT1A5 was added gene: UGT1A5 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: UGT1A5 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: UGT1A5 were set to UDP glucuronosyltransferase deficiency |