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| Structural eye disease v0.76 | RBP3 | Nicola Ragge reviewed gene: RBP3: Rating: RED; Mode of pathogenicity: Other - please provide details in the comments; Publications: ; Phenotypes: ?Retinitis pigmentosa 66, 615233; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | RBP3 | Ivone Leong edited their review of gene: RBP3: Changed phenotypes: ?Retinitis pigmentosa 66, 615233 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | RBP3 | Ivone Leong reviewed gene: RBP3: Rating: RED; Mode of pathogenicity: Other - please provide details in the comments; Publications: ; Phenotypes: Leber congenital amaurosis 12, 610612; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | RBP3 |
Ivone Leong Source NHS GMS was added to RBP3. Mode of inheritance for gene RBP3 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes ?Retinitis pigmentosa 66, 615233 for gene: RBP3 |
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| Structural eye disease v0.2 | RBP3 |
Ellen McDonagh gene: RBP3 was added gene: RBP3 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: RBP3 was set to Phenotypes for gene: RBP3 were set to Eye Disorders |
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