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| Structural eye disease v0.76 | FLVCR1 | Nicola Ragge reviewed gene: FLVCR1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Ataxia, posterior column, with retinitis pigmentosa, 609033; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | FLVCR1 | Ivone Leong reviewed gene: FLVCR1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Ataxia, posterior column, with retinitis pigmentosa, 609033; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | FLVCR1 |
Ivone Leong Source NHS GMS was added to FLVCR1. Mode of inheritance for gene FLVCR1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Ataxia, posterior column, with retinitis pigmentosa, 609033 for gene: FLVCR1 |
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| Structural eye disease v0.2 | FLVCR1 |
Ellen McDonagh gene: FLVCR1 was added gene: FLVCR1 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: FLVCR1 was set to Phenotypes for gene: FLVCR1 were set to Eye Disorders |
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