| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Structural eye disease v0.91 | FANCE | Nicola Ragge reviewed gene: FANCE: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.89 | FANCE |
Ivone Leong Source NHS GMS was added to FANCE. Source Expert Review Red was added to FANCE. Rating Changed from Amber List (moderate evidence) to Red List (low evidence) |
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| Structural eye disease v0.88 | FANCE |
Ivone Leong Source Expert Review Amber was added to FANCE. Rating Changed from Red List (low evidence) to Amber List (moderate evidence) |
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| Structural eye disease v0.60 | FANCE | Mariya Moosajee reviewed gene: FANCE: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Fanconi Anemia, Complementation Group E, FANCE; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.59 | FANCE |
Ivone Leong gene: FANCE was added gene: FANCE was added to Structural eye disease. Sources: London North GLH Mode of inheritance for gene: FANCE was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: FANCE were set to Fanconi Anemia, Complementation Group E, FANCE, 600901 |
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