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BabyScreen+ newborn screening v1.114 BBS9 Tommy Li Added phenotypes Bardet-Biedl syndrome 9, MIM#615986 for gene: BBS9
BabyScreen+ newborn screening v0.154 BBS9 Zornitza Stark Marked gene: BBS9 as ready
BabyScreen+ newborn screening v0.154 BBS9 Zornitza Stark Gene: bbs9 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.154 BBS9 Zornitza Stark Phenotypes for gene: BBS9 were changed from Bardet-Biedl syndrome to Bardet-Biedl syndrome 9, MIM#615986
BabyScreen+ newborn screening v0.153 BBS9 Zornitza Stark Classified gene: BBS9 as Red List (low evidence)
BabyScreen+ newborn screening v0.153 BBS9 Zornitza Stark Gene: bbs9 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.152 BBS9 Zornitza Stark reviewed gene: BBS9: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Bardet-Biedl syndrome 9, MIM#615986; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 BBS9 Zornitza Stark gene: BBS9 was added
gene: BBS9 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: BBS9 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: BBS9 were set to Bardet-Biedl syndrome