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| Structural eye disease v0.76 | RD3 | Nicola Ragge reviewed gene: RD3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Leber congenital amaurosis 12, 610612; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | RD3 | Ivone Leong edited their review of gene: RD3: Changed phenotypes: Leber congenital amaurosis 12, 610612 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | RD3 | Ivone Leong reviewed gene: RD3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Leber congenital amaurosis 13, 612712; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | RD3 |
Ivone Leong Source NHS GMS was added to RD3. Mode of inheritance for gene RD3 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Leber congenital amaurosis 12, 610612 for gene: RD3 |
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| Structural eye disease v0.2 | RD3 |
Ellen McDonagh gene: RD3 was added gene: RD3 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: RD3 was set to Phenotypes for gene: RD3 were set to Eye Disorders |
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