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BabyScreen+ newborn screening v0.228 LIFR Zornitza Stark edited their review of gene: LIFR: Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.228 LIFR Zornitza Stark Marked gene: LIFR as ready
BabyScreen+ newborn screening v0.228 LIFR Zornitza Stark Gene: lifr has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.228 LIFR Zornitza Stark Phenotypes for gene: LIFR were changed from Stuve-Wiedemann syndrome to Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome, MIM# 601559
BabyScreen+ newborn screening v0.227 LIFR Zornitza Stark edited their review of gene: LIFR: Changed phenotypes: Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome, MIM# 601559
BabyScreen+ newborn screening v0.227 LIFR Zornitza Stark Classified gene: LIFR as Red List (low evidence)
BabyScreen+ newborn screening v0.227 LIFR Zornitza Stark Gene: lifr has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.226 LIFR Zornitza Stark reviewed gene: LIFR: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
BabyScreen+ newborn screening v0.199 LIFR David Amor reviewed gene: LIFR: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Stuve-Wiedemann syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 LIFR Zornitza Stark gene: LIFR was added
gene: LIFR was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: LIFR was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: LIFR were set to Stuve-Wiedemann syndrome