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Genomic newborn screening: BabyScreen+ v0.1710 MYO15A Zornitza Stark Tag deafness tag was added to gene: MYO15A.
Genomic newborn screening: BabyScreen+ v0.407 MYO15A Zornitza Stark Marked gene: MYO15A as ready
Genomic newborn screening: BabyScreen+ v0.407 MYO15A Zornitza Stark Gene: myo15a has been classified as Green List (High Evidence).
Genomic newborn screening: BabyScreen+ v0.407 MYO15A Zornitza Stark Phenotypes for gene: MYO15A were changed from Sensorineural hearing loss to Deafness, autosomal recessive 3, MIM# 600316
Genomic newborn screening: BabyScreen+ v0.406 MYO15A Zornitza Stark reviewed gene: MYO15A: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Deafness, autosomal recessive 3, MIM# 600316; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.274 MYO15A David Amor reviewed gene: MYO15A: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Deafness, autosomal recessive 3; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.0 MYO15A Zornitza Stark gene: MYO15A was added
gene: MYO15A was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: MYO15A was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: MYO15A were set to Sensorineural hearing loss