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Factor VIII deficiency v1.2 F8 Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIM #306700) and the OMIM record was last accessed on 18 December 2025.
Factor VIII deficiency v1.2 F8 Achchuthan Shanmugasundram Phenotypes for gene: F8 were changed from to Hemophilia A, OMIM:306700; hemophilia A, MONDO:0010602
Factor VIII deficiency v1.1 Eleanor Williams Panel version 1.0 has been signed off on 2023-09-14
Factor VIII deficiency v1.0 Eleanor Williams promoted panel to version 1.0
Factor VIII deficiency v0.3 Eleanor Williams Panel types changed to GMS Rare Disease; GMS signed-off
Factor VIII deficiency v0.2 Achchuthan Shanmugasundram Panel status changed from internal to public
Factor VIII deficiency v0.1 F8 Achchuthan Shanmugasundram reviewed gene: F8: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Factor VIII deficiency v0.1 F8 Achchuthan Shanmugasundram gene: F8 was added
gene: F8 was added to Factor VIII deficiency. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: F8 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Factor VIII deficiency v0.0 Achchuthan Shanmugasundram Added Panel Factor VIII deficiency
Set list of related panels to R117
Set panel types to: GMS Rare Disease