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Factor XI deficiency v1.2 F11 Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIM #612416) and the OMIM record was last accessed on 18 December 2025.
Factor XI deficiency v1.2 F11 Achchuthan Shanmugasundram Phenotypes for gene: F11 were changed from to Factor XI deficiency, autosomal dominant, OMIM:612416; Factor XI deficiency, autosomal recessive, OMIM:612416; congenital factor XI deficiency, MONDO:0012897
Factor XI deficiency v1.1 Eleanor Williams Panel version 1.0 has been signed off on 2023-09-14
Factor XI deficiency v1.0 Eleanor Williams promoted panel to version 1.0
Factor XI deficiency v0.3 Eleanor Williams Panel types changed to GMS Rare Disease; GMS signed-off
Factor XI deficiency v0.2 Achchuthan Shanmugasundram Panel status changed from internal to public
Factor XI deficiency v0.1 F11 Achchuthan Shanmugasundram reviewed gene: F11: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Factor XI deficiency v0.1 F11 Achchuthan Shanmugasundram gene: F11 was added
gene: F11 was added to Factor XI deficiency. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: F11 was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Factor XI deficiency v0.0 Achchuthan Shanmugasundram Added Panel Factor XI deficiency
Set list of related panels to R120
Set panel types to: GMS Rare Disease