Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Factor XIII deficiency v1.1 | Eleanor Williams Panel version 1.0 has been signed off on 2023-09-14 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Factor XIII deficiency v1.0 | Eleanor Williams promoted panel to version 1.0 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Factor XIII deficiency v0.3 | Eleanor Williams Panel types changed to GMS Rare Disease; GMS signed-off | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Factor XIII deficiency v0.2 | Achchuthan Shanmugasundram Panel status changed from internal to public | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Factor XIII deficiency v0.1 | F13B | Achchuthan Shanmugasundram reviewed gene: F13B: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Factor XIII deficiency v0.1 | F13A1 | Achchuthan Shanmugasundram reviewed gene: F13A1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Factor XIII deficiency v0.1 | F13B |
Achchuthan Shanmugasundram gene: F13B was added gene: F13B was added to Factor XIII deficiency. Sources: Expert Review Green,NHS GMS Mode of inheritance for gene: F13B was set to BIALLELIC, autosomal or pseudoautosomal |
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Factor XIII deficiency v0.1 | F13A1 |
Achchuthan Shanmugasundram gene: F13A1 was added gene: F13A1 was added to Factor XIII deficiency. Sources: Expert Review Green,NHS GMS Mode of inheritance for gene: F13A1 was set to BIALLELIC, autosomal or pseudoautosomal |
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Factor XIII deficiency v0.0 |
Achchuthan Shanmugasundram Added Panel Factor XIII deficiency Set list of related panels to R122 Set panel types to: GMS Rare Disease |