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| Additional findings_Paediatric v0.2 | LBR |
Zornitza Stark Source BabySeq Category C gene was added to LBR. Source Expert Review Red was added to LBR. Mode of inheritance for gene LBR was changed from BIALLELIC, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Reynolds syndrome for gene: LBR Rating Changed from Green List (high evidence) to Red List (low evidence) |
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| Additional findings_Paediatric v0.2 | LBR |
Zornitza Stark gene: LBR was added gene: LBR was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene Mode of inheritance for gene: LBR was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: LBR were set to Pelger-Huet anomaly |
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