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Genomic newborn screening: BabyScreen+ v0.340 MKKS Zornitza Stark Marked gene: MKKS as ready
Genomic newborn screening: BabyScreen+ v0.340 MKKS Zornitza Stark Gene: mkks has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.340 MKKS Zornitza Stark Phenotypes for gene: MKKS were changed from Bardet-Biedl syndrome to Bardet-Biedl syndrome 6 (MIM#605231); McKusick-Kaufman syndrome, MIM# 236700
Genomic newborn screening: BabyScreen+ v0.339 MKKS Zornitza Stark Classified gene: MKKS as Red List (low evidence)
Genomic newborn screening: BabyScreen+ v0.339 MKKS Zornitza Stark Gene: mkks has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.338 MKKS Zornitza Stark reviewed gene: MKKS: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Bardet-Biedl syndrome 6 (MIM#605231), McKusick-Kaufman syndrome, MIM# 236700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.270 MKKS David Amor reviewed gene: MKKS: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: McKusick-Kaufman syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.0 MKKS Zornitza Stark gene: MKKS was added
gene: MKKS was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: MKKS was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: MKKS were set to Bardet-Biedl syndrome