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| Structural eye disease v0.91 | ALX3 | Nicola Ragge reviewed gene: ALX3: Rating: RED; Mode of pathogenicity: ; Publications: 19409524; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.89 | ALX3 |
Ivone Leong Source NHS GMS was added to ALX3. Source Expert Review Red was added to ALX3. Publications for gene ALX3 were changed from to 19409524 Rating Changed from Amber List (moderate evidence) to Red List (low evidence) |
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| Structural eye disease v0.86 | ALX3 | Ivone Leong Classified gene: ALX3 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.86 | ALX3 | Ivone Leong Gene: alx3 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.60 | ALX3 | Mariya Moosajee reviewed gene: ALX3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Frontonasal Dysplasia 1, FND1; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.59 | ALX3 |
Ivone Leong gene: ALX3 was added gene: ALX3 was added to Structural eye disease. Sources: London North GLH Mode of inheritance for gene: ALX3 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ALX3 were set to Frontonasal Dysplasia 1, FND1, 136760 |
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