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Thrombophilia with a likely monogenic cause v0.37 F3 Louise Daugherty commented on gene: F3: Follow up email correspondence with Patricia Bignell 13th March (webex 8.03.19 WWMGLH comments v1.doc), on behalf of Wessex and the West Midlands GLH for the GMS Haematology specialist test group, suggested rating Red
Thrombophilia with a likely monogenic cause v0.36 F3 Louise Daugherty Source Wessex and West Midlands GLH was added to F3.
Thrombophilia with a likely monogenic cause v0.35 F3 PATRICIA BIGNELL reviewed gene: F3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Thrombophilia with a likely monogenic cause v0.16 F3 Louise Daugherty Phenotypes for gene: F3 were changed from No OMIM number; Tissue factor deficiency (Factor III) to Tissue factor deficiency (Factor III)
Thrombophilia with a likely monogenic cause v0.15 F3 Louise Daugherty Mode of inheritance for gene: F3 was changed from BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Thrombophilia with a likely monogenic cause v0.14 F3 Louise Daugherty Mode of inheritance for gene: F3 was changed from to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Thrombophilia with a likely monogenic cause v0.13 F3 Louise Daugherty Classified gene: F3 as Amber List (moderate evidence)
Thrombophilia with a likely monogenic cause v0.13 F3 Louise Daugherty Gene: f3 has been classified as Amber List (Moderate Evidence).
Thrombophilia with a likely monogenic cause v0.12 F3 Louise Daugherty reviewed gene: F3: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Thrombophilia with a likely monogenic cause v0.11 F3 Michael Mitchell reviewed gene: F3: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: Tissue factor deficiency (Factor III), No OMIM number; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Thrombophilia with a likely monogenic cause v0.10 F3 Louise Daugherty Added phenotypes No OMIM number; Tissue factor deficiency (Factor III) for gene: F3
Thrombophilia with a likely monogenic cause v0.9 F3 Louise Daugherty Source NHS GMS was added to F3.
Thrombophilia with a likely monogenic cause v0.8 F3 Louise Daugherty gene: F3 was added
gene: F3 was added to Thrombophilia. Sources: London South GLH
Mode of inheritance for gene: F3 was set to