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| Structural eye disease v0.76 | RDH5 | Nicola Ragge reviewed gene: RDH5: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Fundus albipunctatus, 136880; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | RDH5 | Ivone Leong edited their review of gene: RDH5: Changed phenotypes: Fundus albipunctatus, 136880 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | RDH5 | Ivone Leong reviewed gene: RDH5: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 44, 613769; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | RDH5 |
Ivone Leong Source NHS GMS was added to RDH5. Mode of inheritance for gene RDH5 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Fundus albipunctatus, 136880 for gene: RDH5 |
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| Structural eye disease v0.2 | RDH5 |
Ellen McDonagh gene: RDH5 was added gene: RDH5 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: RDH5 was set to Phenotypes for gene: RDH5 were set to Eye Disorders |
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