Activity

Filter

Cancel
Date Panel Item Activity
8 actions
Bleeding and Platelet Disorders v0.16 FBN2 Zornitza Stark Marked gene: FBN2 as ready
Bleeding and Platelet Disorders v0.16 FBN2 Zornitza Stark Gene: fbn2 has been classified as Red List (Low Evidence).
Bleeding and Platelet Disorders v0.16 FBN2 Zornitza Stark Phenotypes for gene: FBN2 were changed from to Contractural arachnodactyly, congenital 121050; Macular degeneration, early-onset 616118
Bleeding and Platelet Disorders v0.15 FBN2 Zornitza Stark Mode of inheritance for gene: FBN2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Bleeding and Platelet Disorders v0.14 FBN2 Zornitza Stark Classified gene: FBN2 as Red List (low evidence)
Bleeding and Platelet Disorders v0.14 FBN2 Zornitza Stark Gene: fbn2 has been classified as Red List (Low Evidence).
Bleeding and Platelet Disorders v0.13 FBN2 Zornitza Stark reviewed gene: FBN2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Contractural arachnodactyly, congenital 121050, Macular degeneration, early-onset 616118; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Bleeding and Platelet Disorders v0.0 FBN2 Zornitza Stark gene: FBN2 was added
gene: FBN2 was added to Bleeding Disorders_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: FBN2 was set to Unknown