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BabyScreen+ newborn screening v1.114 VHL Tommy Li Added phenotypes von Hippel-Lindau syndrome MIM#193300 for gene: VHL
Publications for gene VHL were updated from 20301636; 33945366; 34613603; 28620007 to 33945366; 34613603; 20301636; 28620007
BabyScreen+ newborn screening v0.1632 VHL Zornitza Stark Tag cancer tag was added to gene: VHL.
BabyScreen+ newborn screening v0.728 VHL Zornitza Stark Publications for gene: VHL were set to 20301636; 33945366; 34613603
BabyScreen+ newborn screening v0.727 VHL Zornitza Stark Tag for review was removed from gene: VHL.
Tag treatable tag was added to gene: VHL.
BabyScreen+ newborn screening v0.727 VHL Zornitza Stark edited their review of gene: VHL: Changed publications: 28620007
BabyScreen+ newborn screening v0.727 VHL Zornitza Stark reviewed gene: VHL: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: von Hippel-Lindau syndrome MIM#193300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
BabyScreen+ newborn screening v0.617 VHL Zornitza Stark Marked gene: VHL as ready
BabyScreen+ newborn screening v0.617 VHL Zornitza Stark Gene: vhl has been classified as Green List (High Evidence).
BabyScreen+ newborn screening v0.617 VHL Zornitza Stark Publications for gene: VHL were set to
BabyScreen+ newborn screening v0.616 VHL Zornitza Stark Phenotypes for gene: VHL were changed from von Hippel-Lindau syndrome to von Hippel-Lindau syndrome MIM#193300
BabyScreen+ newborn screening v0.615 VHL Zornitza Stark Tag for review tag was added to gene: VHL.
BabyScreen+ newborn screening v0.604 VHL Lilian Downie reviewed gene: VHL: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 20301636, PMID: 33945366, PMID: 34613603; Phenotypes: von Hippel-Lindau syndrome MIM#193300; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
BabyScreen+ newborn screening v0.0 VHL Zornitza Stark gene: VHL was added
gene: VHL was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: VHL was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: VHL were set to von Hippel-Lindau syndrome