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| Structural eye disease v0.76 | RDH12 | Nicola Ragge reviewed gene: RDH12: Rating: RED; Mode of pathogenicity: ; Publications: 25148430, 22065924; Phenotypes: Leber congenital amaurosis 13, 612712; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | RDH12 | Ivone Leong edited their review of gene: RDH12: Changed phenotypes: Leber congenital amaurosis 13, 612712 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | RDH12 | Ivone Leong reviewed gene: RDH12: Rating: RED; Mode of pathogenicity: ; Publications: 25148430, 22065924; Phenotypes: Fundus albipunctatus, 136880; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | RDH12 |
Ivone Leong Source NHS GMS was added to RDH12. Mode of inheritance for gene RDH12 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Leber congenital amaurosis 13, 612712 for gene: RDH12 Publications for gene RDH12 were changed from to 25148430; 22065924 |
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| Structural eye disease v0.2 | RDH12 |
Ellen McDonagh gene: RDH12 was added gene: RDH12 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: RDH12 was set to Phenotypes for gene: RDH12 were set to Eye Disorders |
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