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| Structural eye disease v0.76 | IMPG2 | Nicola Ragge reviewed gene: IMPG2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 56, Macular dystrophy, vitelliform, 5, 613581, 616152; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | IMPG2 | Ivone Leong reviewed gene: IMPG2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 56, 613581, Macular dystrophy, vitelliform, 5, 616152; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | IMPG2 |
Ivone Leong Source NHS GMS was added to IMPG2. Mode of inheritance for gene IMPG2 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Retinitis pigmentosa 56, 613581; Macular dystrophy, vitelliform, 5, 616152 for gene: IMPG2 |
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| Structural eye disease v0.2 | IMPG2 |
Ellen McDonagh gene: IMPG2 was added gene: IMPG2 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: IMPG2 was set to Phenotypes for gene: IMPG2 were set to Eye Disorders |
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