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| Structural eye disease v0.76 | CNGB3 | Nicola Ragge reviewed gene: CNGB3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Macular degeneration, juvenile, Achromatopsia-3, 248200, 262300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | CNGB3 | Ivone Leong reviewed gene: CNGB3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Macular degeneration, juvenile, 248200, Achromatopsia-3, 262300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | CNGB3 |
Ivone Leong Source NHS GMS was added to CNGB3. Mode of inheritance for gene CNGB3 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Achromatopsia-3, 262300; Macular degeneration, juvenile, 248200 for gene: CNGB3 |
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| Structural eye disease v0.2 | CNGB3 |
Ellen McDonagh gene: CNGB3 was added gene: CNGB3 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: CNGB3 was set to Phenotypes for gene: CNGB3 were set to Eye Disorders |
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