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| Structural eye disease v0.76 | USH1G | Nicola Ragge reviewed gene: USH1G: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Usher syndrome, type 1G, 606943; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | USH1G | Ivone Leong edited their review of gene: USH1G: Changed phenotypes: Usher syndrome, type 1G, 606943 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | USH1G | Ivone Leong reviewed gene: USH1G: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 39, 613809, Usher syndrome type 2A, 276901; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | USH1G |
Ivone Leong Source NHS GMS was added to USH1G. Mode of inheritance for gene USH1G was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Usher syndrome, type 1G, 606943 for gene: USH1G |
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| Structural eye disease v0.2 | USH1G |
Ellen McDonagh gene: USH1G was added gene: USH1G was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: USH1G was set to Phenotypes for gene: USH1G were set to Eye Disorders |
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