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| Structural eye disease v0.76 | IDH3B | Nicola Ragge reviewed gene: IDH3B: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 46, 612572; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | IDH3B | Ivone Leong reviewed gene: IDH3B: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 46, 612572; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | IDH3B |
Ivone Leong Source NHS GMS was added to IDH3B. Mode of inheritance for gene IDH3B was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Retinitis pigmentosa 46, 612572 for gene: IDH3B |
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| Structural eye disease v0.2 | IDH3B |
Ellen McDonagh gene: IDH3B was added gene: IDH3B was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: IDH3B was set to Phenotypes for gene: IDH3B were set to Eye Disorders |
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