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| Structural eye disease v0.76 | PRPF8 | Nicola Ragge reviewed gene: PRPF8: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 13, 600059; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | PRPF8 | Ivone Leong edited their review of gene: PRPF8: Changed phenotypes: Retinitis pigmentosa 13, 600059 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | PRPF8 | Ivone Leong reviewed gene: PRPF8: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis punctata albescens, 136880, Macular dystrophy, patterned, 1, 169150, Leber congenital amaurosis 18, 608133, Macular dystrophy, vitelliform, 3, 608161, Choriodal dystrophy, central areolar 2, 613105; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | PRPF8 |
Ivone Leong Source NHS GMS was added to PRPF8. Mode of inheritance for gene PRPF8 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Retinitis pigmentosa 13, 600059 for gene: PRPF8 |
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| Structural eye disease v0.2 | PRPF8 |
Ellen McDonagh gene: PRPF8 was added gene: PRPF8 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: PRPF8 was set to Phenotypes for gene: PRPF8 were set to Eye Disorders |
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