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BabyScreen+ newborn screening v0.235 LMOD3 Zornitza Stark Marked gene: LMOD3 as ready
BabyScreen+ newborn screening v0.235 LMOD3 Zornitza Stark Gene: lmod3 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.235 LMOD3 Zornitza Stark Phenotypes for gene: LMOD3 were changed from Nemaline myopathy to Nemaline myopathy 10, MIM# 616165
BabyScreen+ newborn screening v0.234 LMOD3 Zornitza Stark Classified gene: LMOD3 as Red List (low evidence)
BabyScreen+ newborn screening v0.234 LMOD3 Zornitza Stark Gene: lmod3 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.233 LMOD3 Zornitza Stark reviewed gene: LMOD3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Nemaline myopathy 10, MIM# 616165; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.200 LMOD3 David Amor edited their review of gene: LMOD3: Changed rating: GREEN
BabyScreen+ newborn screening v0.200 LMOD3 David Amor reviewed gene: LMOD3: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: Nemaline myopathy 10; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 LMOD3 Zornitza Stark gene: LMOD3 was added
gene: LMOD3 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: LMOD3 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: LMOD3 were set to Nemaline myopathy