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Genomic newborn screening: BabyScreen+ v0.298 CHRNG Zornitza Stark Marked gene: CHRNG as ready
Genomic newborn screening: BabyScreen+ v0.298 CHRNG Zornitza Stark Gene: chrng has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.298 CHRNG Zornitza Stark Phenotypes for gene: CHRNG were changed from Pterygium syndrome to Escobar syndrome, MIM# 265000; Multiple pterygium syndrome, lethal type, MIM# 253290
Genomic newborn screening: BabyScreen+ v0.297 CHRNG Zornitza Stark Classified gene: CHRNG as Red List (low evidence)
Genomic newborn screening: BabyScreen+ v0.297 CHRNG Zornitza Stark Gene: chrng has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.296 CHRNG Zornitza Stark reviewed gene: CHRNG: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Escobar syndrome, MIM# 265000, Multiple pterygium syndrome, lethal type, MIM# 253290; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.266 CHRNG John Christodoulou reviewed gene: CHRNG: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.0 CHRNG Zornitza Stark gene: CHRNG was added
gene: CHRNG was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: CHRNG was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: CHRNG were set to Pterygium syndrome