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| Structural eye disease v0.91 | FANCD2 | Nicola Ragge reviewed gene: FANCD2: Rating: RED; Mode of pathogenicity: ; Publications: 12893777; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.89 | FANCD2 |
Ivone Leong Source NHS GMS was added to FANCD2. Source Expert Review Red was added to FANCD2. Publications for gene FANCD2 were changed from to 12893777 Rating Changed from Amber List (moderate evidence) to Red List (low evidence) |
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| Structural eye disease v0.88 | FANCD2 |
Ivone Leong Source Expert Review Amber was added to FANCD2. Rating Changed from Red List (low evidence) to Amber List (moderate evidence) |
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| Structural eye disease v0.60 | FANCD2 | Mariya Moosajee reviewed gene: FANCD2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Fanconi Anemia, Complementation Group D2, FANCD2; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.59 | FANCD2 |
Ivone Leong gene: FANCD2 was added gene: FANCD2 was added to Structural eye disease. Sources: London North GLH Mode of inheritance for gene: FANCD2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: FANCD2 were set to Fanconi Anemia, Complementation Group D2, FANCD2, 227646 |
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