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BabyScreen+ newborn screening v0.910 ELP1 Zornitza Stark Marked gene: ELP1 as ready
BabyScreen+ newborn screening v0.910 ELP1 Zornitza Stark Gene: elp1 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.910 ELP1 Zornitza Stark Phenotypes for gene: ELP1 were changed from Dysautonomia, familial to Dysautonomia, familial MIM#223900; paediatric medulloblastoma
BabyScreen+ newborn screening v0.909 ELP1 Zornitza Stark Mode of inheritance for gene: ELP1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.908 ELP1 Zornitza Stark Classified gene: ELP1 as Red List (low evidence)
BabyScreen+ newborn screening v0.908 ELP1 Zornitza Stark Gene: elp1 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.907 ELP1 Zornitza Stark reviewed gene: ELP1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Dysautonomia, familial MIM#223900, paediatric medulloblastoma; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 ELP1 Zornitza Stark gene: ELP1 was added
gene: ELP1 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: ELP1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ELP1 were set to Dysautonomia, familial