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| Structural eye disease v0.76 | USH2A | Nicola Ragge reviewed gene: USH2A: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 39, Usher syndrome type 2A, 613809, 276901; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | USH2A | Ivone Leong edited their review of gene: USH2A: Changed phenotypes: Retinitis pigmentosa 39, 613809, Usher syndrome type 2A, 276901 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | USH2A | Ivone Leong reviewed gene: USH2A: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Microphthalmia, syndromic 11, 614402; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | USH2A |
Ivone Leong Source NHS GMS was added to USH2A. Mode of inheritance for gene USH2A was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Usher syndrome type 2A, 276901; Retinitis pigmentosa 39, 613809 for gene: USH2A |
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| Structural eye disease v0.2 | USH2A |
Ellen McDonagh gene: USH2A was added gene: USH2A was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: USH2A was set to Phenotypes for gene: USH2A were set to Eye Disorders |
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