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| Structural eye disease v0.76 | NR2E3 | Nicola Ragge reviewed gene: NR2E3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 37, Enhanced S-cone syndrome, 611131, 268100; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | NR2E3 | Ivone Leong edited their review of gene: NR2E3: Changed phenotypes: Retinitis pigmentosa 37, 611131, Enhanced S-cone syndrome, 268100 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | NR2E3 | Ivone Leong reviewed gene: NR2E3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 27, 613750; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | NR2E3 |
Ivone Leong Source NHS GMS was added to NR2E3. Mode of inheritance for gene NR2E3 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Added phenotypes Enhanced S-cone syndrome, 268100; Retinitis pigmentosa 37, 611131 for gene: NR2E3 |
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| Structural eye disease v0.2 | NR2E3 |
Ellen McDonagh gene: NR2E3 was added gene: NR2E3 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: NR2E3 was set to Phenotypes for gene: NR2E3 were set to Eye Disorders |
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