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BabyScreen+ newborn screening v0.1121 GSS Zornitza Stark Marked gene: GSS as ready
BabyScreen+ newborn screening v0.1121 GSS Zornitza Stark Gene: gss has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.1121 GSS Zornitza Stark Phenotypes for gene: GSS were changed from Glutathione synthetase deficiency to Glutathione synthetase deficiency, MIM# 266130; Haemolytic anemia due to glutathione synthetase deficiency 231900
BabyScreen+ newborn screening v0.1120 GSS Zornitza Stark Classified gene: GSS as Red List (low evidence)
BabyScreen+ newborn screening v0.1120 GSS Zornitza Stark Gene: gss has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.1119 GSS Zornitza Stark reviewed gene: GSS: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Glutathione synthetase deficiency, MIM# 266130, Haemolytic anemia due to glutathione synthetase deficiency 231900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 GSS Zornitza Stark gene: GSS was added
gene: GSS was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: GSS was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: GSS were set to Glutathione synthetase deficiency