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| Structural eye disease v0.76 | CNGA3 | Nicola Ragge reviewed gene: CNGA3: Rating: RED; Mode of pathogenicity: ; Publications: 24504161; Phenotypes: Achromatopsia-2, 216900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | CNGA3 | Ivone Leong reviewed gene: CNGA3: Rating: RED; Mode of pathogenicity: ; Publications: 24504161; Phenotypes: Achromatopsia-2, 216900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | CNGA3 |
Ivone Leong Source NHS GMS was added to CNGA3. Mode of inheritance for gene CNGA3 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Achromatopsia-2, 216900 for gene: CNGA3 Publications for gene CNGA3 were changed from to 24504161 |
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| Structural eye disease v0.2 | CNGA3 |
Ellen McDonagh gene: CNGA3 was added gene: CNGA3 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: CNGA3 was set to Phenotypes for gene: CNGA3 were set to Eye Disorders |
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