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BabyScreen+ newborn screening v1.114 PPT1 Tommy Li Added phenotypes Ceroid lipofuscinosis, neuronal, 1, MIM# 256730 for gene: PPT1
BabyScreen+ newborn screening v0.1619 PPT1 Zornitza Stark Marked gene: PPT1 as ready
BabyScreen+ newborn screening v0.1619 PPT1 Zornitza Stark Gene: ppt1 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.1619 PPT1 Zornitza Stark Publications for gene: PPT1 were set to
BabyScreen+ newborn screening v0.1618 PPT1 Zornitza Stark Phenotypes for gene: PPT1 were changed from Neuronal ceroid lipofuscinosis to Ceroid lipofuscinosis, neuronal, 1, MIM# 256730
BabyScreen+ newborn screening v0.1617 PPT1 Zornitza Stark Classified gene: PPT1 as Red List (low evidence)
BabyScreen+ newborn screening v0.1617 PPT1 Zornitza Stark Gene: ppt1 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.1606 PPT1 John Christodoulou reviewed gene: PPT1: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 21990111; Phenotypes: neurodegeneration, seizures, ataxia, optic atrophy, retinal abnormalities; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 PPT1 Zornitza Stark gene: PPT1 was added
gene: PPT1 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: PPT1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: PPT1 were set to Neuronal ceroid lipofuscinosis