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Genomic newborn screening: BabyScreen+ v0.528 CTSD Zornitza Stark Marked gene: CTSD as ready
Genomic newborn screening: BabyScreen+ v0.528 CTSD Zornitza Stark Gene: ctsd has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.528 CTSD Zornitza Stark Phenotypes for gene: CTSD were changed from Ceroid lipofuscinosis, neuronal, 10 to Ceroid lipofuscinosis, neuronal, 10, MIM# 610127
Genomic newborn screening: BabyScreen+ v0.527 CTSD Zornitza Stark Classified gene: CTSD as Red List (low evidence)
Genomic newborn screening: BabyScreen+ v0.527 CTSD Zornitza Stark Gene: ctsd has been classified as Red List (Low Evidence).
Genomic newborn screening: BabyScreen+ v0.526 CTSD Zornitza Stark reviewed gene: CTSD: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ceroid lipofuscinosis, neuronal, 10, MIM# 610127; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.523 CTSD John Christodoulou reviewed gene: CTSD: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: neuronal ceroid lipofuscinosis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genomic newborn screening: BabyScreen+ v0.0 CTSD Zornitza Stark gene: CTSD was added
gene: CTSD was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: CTSD was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: CTSD were set to Ceroid lipofuscinosis, neuronal, 10