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Severe Paediatric Disorders v0.17 FBN2 Louise Daugherty Mode of inheritance for gene FBN2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Severe Paediatric Disorders v0.12 FBN2 Louise Daugherty reviewed gene: FBN2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 FBN2 Louise Daugherty Publications for gene FBN2 were updated from to 30847515
Severe Paediatric Disorders v0.10 FBN2 Louise Daugherty Added phenotypes Macular degeneration, early-onset, 616118; Contractural arachnodactyly, congenital, 121050 for gene: FBN2
Severe Paediatric Disorders v0.9 FBN2 Louise Daugherty Added phenotypes Macular degeneration, early-onset, 616118; Contractural arachnodactyly, congenital, 121050 for gene: FBN2
Severe Paediatric Disorders v0.9 FBN2 Louise Daugherty Added phenotypes Macular degeneration, early-onset, 616118; Contractural arachnodactyly, congenital, 121050 for gene: FBN2
Severe Paediatric Disorders v0.8 FBN2 Louise Daugherty Added phenotypes Contractural arachnodactyly, congenital, 121050; Macular degeneration, early-onset, 616118 for gene: FBN2
Severe Paediatric Disorders v0.7 FBN2 Louise Daugherty Source Next Generation Children Project was added to FBN2.
Severe Paediatric Disorders v0.5 FBN2 Louise Daugherty Source Expert Review Green was added to FBN2.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 FBN2 Louise Daugherty gene: FBN2 was added
gene: FBN2 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: FBN2 was set to