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BabyScreen+ newborn screening v0.328 MFSD8 Zornitza Stark Marked gene: MFSD8 as ready
BabyScreen+ newborn screening v0.328 MFSD8 Zornitza Stark Gene: mfsd8 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.328 MFSD8 Zornitza Stark Phenotypes for gene: MFSD8 were changed from Ceroid lipofuscinosis, neuronal to Ceroid lipofuscinosis, neuronal, 7, MIM# 610951
BabyScreen+ newborn screening v0.327 MFSD8 Zornitza Stark Publications for gene: MFSD8 were set to
BabyScreen+ newborn screening v0.326 MFSD8 Zornitza Stark Classified gene: MFSD8 as Red List (low evidence)
BabyScreen+ newborn screening v0.326 MFSD8 Zornitza Stark Gene: mfsd8 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.325 MFSD8 Zornitza Stark reviewed gene: MFSD8: Rating: RED; Mode of pathogenicity: None; Publications: 31597037; Phenotypes: Ceroid lipofuscinosis, neuronal, 7, MIM# 610951; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.270 MFSD8 David Amor reviewed gene: MFSD8: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: neuronal ceroid lipofuscinosis-7 (CLN7); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 MFSD8 Zornitza Stark gene: MFSD8 was added
gene: MFSD8 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: MFSD8 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: MFSD8 were set to Ceroid lipofuscinosis, neuronal