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Structural eye disease v0.91 | FANCI | Nicola Ragge reviewed gene: FANCI: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.89 | FANCI |
Ivone Leong Source NHS GMS was added to FANCI. Source Expert Review Red was added to FANCI. Rating Changed from Amber List (moderate evidence) to Red List (low evidence) |
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Structural eye disease v0.88 | FANCI |
Ivone Leong Source Expert Review Amber was added to FANCI. Rating Changed from Red List (low evidence) to Amber List (moderate evidence) |
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Structural eye disease v0.60 | FANCI | Mariya Moosajee reviewed gene: FANCI: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Fanconi Anemia, Complementation Group I, FANCI; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.59 | FANCI |
Ivone Leong gene: FANCI was added gene: FANCI was added to Structural eye disease. Sources: London North GLH Mode of inheritance for gene: FANCI was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: FANCI were set to Fanconi Anemia, Complementation Group I, FANCI, 609053 |