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BabyScreen+ newborn screening v1.114 MTHFR Tommy Li Added phenotypes Homocystinuria due to MTHFR deficiency MIM#236250 for gene: MTHFR
BabyScreen+ newborn screening v0.1906 MTHFR Zornitza Stark Marked gene: MTHFR as ready
BabyScreen+ newborn screening v0.1906 MTHFR Zornitza Stark Gene: mthfr has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.1906 MTHFR Zornitza Stark Phenotypes for gene: MTHFR were changed from Homocystinuria due to MTHFR deficiency to Homocystinuria due to MTHFR deficiency MIM#236250
BabyScreen+ newborn screening v0.1905 MTHFR Zornitza Stark Publications for gene: MTHFR were set to
BabyScreen+ newborn screening v0.1904 MTHFR Zornitza Stark Classified gene: MTHFR as Red List (low evidence)
BabyScreen+ newborn screening v0.1904 MTHFR Zornitza Stark Gene: mthfr has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.1883 MTHFR Lilian Downie reviewed gene: MTHFR: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 34214447; Phenotypes: Homocystinuria due to MTHFR deficiency MIM#236250; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 MTHFR Zornitza Stark gene: MTHFR was added
gene: MTHFR was added to gNBS. Sources: Expert Review Amber,BabySeq Category B gene
Mode of inheritance for gene: MTHFR was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: MTHFR were set to Homocystinuria due to MTHFR deficiency