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BabyScreen+ newborn screening v1.114 TTR Tommy Li Added phenotypes Amyloidosis, hereditary, transthyretin-related MIM#105210 for gene: TTR
Publications for gene TTR were updated from 20301373; 3032328; 29972753; 29972757 to 3032328; 29972753; 29972757; 20301373
BabyScreen+ newborn screening v0.811 TTR Zornitza Stark Marked gene: TTR as ready
BabyScreen+ newborn screening v0.811 TTR Zornitza Stark Gene: ttr has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.811 TTR Zornitza Stark Phenotypes for gene: TTR were changed from Amyloidosis, hereditary, transthyretin-related to Amyloidosis, hereditary, transthyretin-related MIM#105210
BabyScreen+ newborn screening v0.810 TTR Zornitza Stark Publications for gene: TTR were set to
BabyScreen+ newborn screening v0.809 TTR Zornitza Stark Classified gene: TTR as Red List (low evidence)
BabyScreen+ newborn screening v0.809 TTR Zornitza Stark Gene: ttr has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.802 TTR Lilian Downie reviewed gene: TTR: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 20301373, PMID: 3032328, PMID: 29972753, PMID: 29972757; Phenotypes: Amyloidosis, hereditary, transthyretin-related MIM#105210; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
BabyScreen+ newborn screening v0.0 TTR Zornitza Stark gene: TTR was added
gene: TTR was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: TTR was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: TTR were set to Amyloidosis, hereditary, transthyretin-related