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Additional findings_Paediatric v0.2 ALG11 Zornitza Stark gene: ALG11 was added
gene: ALG11 was added to Newborn Screening_BabySeq. Sources: BabySeq Category C gene,Expert Review Red
Mode of inheritance for gene: ALG11 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ALG11 were set to Congenital disorder of glycosylation type 1P
Additional findings_Paediatric v0.2 ALG12 Zornitza Stark Added phenotypes Congenital disorder of glycosylation, type Ig for gene: ALG12
Additional findings_Paediatric v0.2 ALG1 Zornitza Stark Added phenotypes Congenital disorder of glycosylation, type Ik for gene: ALG1
Additional findings_Paediatric v0.0 ALG12 Zornitza Stark gene: ALG12 was added
gene: ALG12 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene
Mode of inheritance for gene: ALG12 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ALG12 were set to Congenital disorder of glycosylation, type Ig
Additional findings_Paediatric v0.0 ALG1 Zornitza Stark gene: ALG1 was added
gene: ALG1 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene
Mode of inheritance for gene: ALG1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ALG1 were set to Congenital disorder of glycosylation, type Ik