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BabyScreen+ newborn screening v1.114 LAMA2 Tommy Li Added phenotypes Muscular dystrophy, congenital, merosin deficient or partially deficient, MIM# 607855 for gene: LAMA2
BabyScreen+ newborn screening v0.865 LAMA2 Zornitza Stark Classified gene: LAMA2 as Green List (high evidence)
BabyScreen+ newborn screening v0.865 LAMA2 Zornitza Stark Gene: lama2 has been classified as Green List (High Evidence).
BabyScreen+ newborn screening v0.864 LAMA2 Zornitza Stark Tag pharmacogenomic tag was added to gene: LAMA2.
BabyScreen+ newborn screening v0.864 LAMA2 Zornitza Stark edited their review of gene: LAMA2: Changed rating: GREEN
BabyScreen+ newborn screening v0.864 LAMA2 Zornitza Stark changed review comment from: No specific treatment.; to: No specific treatment.
Succinylcholine in induction of anaesthesia because of risk of hyperkalaemia and cardiac conduction abnormalities; statins, cholesterol-lowering medications, because of the risk of muscle damage.
BabyScreen+ newborn screening v0.864 LAMA2 Zornitza Stark Tag for review was removed from gene: LAMA2.
BabyScreen+ newborn screening v0.335 LAMA2 Zornitza Stark Marked gene: LAMA2 as ready
BabyScreen+ newborn screening v0.335 LAMA2 Zornitza Stark Gene: lama2 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.335 LAMA2 Zornitza Stark Phenotypes for gene: LAMA2 were changed from Muscular dystrophy, congenital merosin-deficient to Muscular dystrophy, congenital, merosin deficient or partially deficient, MIM# 607855
BabyScreen+ newborn screening v0.334 LAMA2 Zornitza Stark Classified gene: LAMA2 as Red List (low evidence)
BabyScreen+ newborn screening v0.334 LAMA2 Zornitza Stark Gene: lama2 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.270 LAMA2 David Amor edited their review of gene: LAMA2: Changed rating: RED
BabyScreen+ newborn screening v0.205 LAMA2 Zornitza Stark Tag for review tag was added to gene: LAMA2.
BabyScreen+ newborn screening v0.205 LAMA2 Zornitza Stark reviewed gene: LAMA2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Muscular dystrophy, congenital, merosin deficient or partially deficient, MIM# 607855; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.199 LAMA2 David Amor reviewed gene: LAMA2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: LAMA2 muscular dystrophy; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 LAMA2 Zornitza Stark gene: LAMA2 was added
gene: LAMA2 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: LAMA2 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: LAMA2 were set to Muscular dystrophy, congenital merosin-deficient