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| Structural eye disease v0.76 | TTC8 | Nicola Ragge reviewed gene: TTC8: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 51, Bardet-Biedl syndrome 8, 613464, 615985; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | TTC8 | Ivone Leong edited their review of gene: TTC8: Changed phenotypes: Retinitis pigmentosa 51, 613464, Bardet-Biedl syndrome 8, 615985 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | TTC8 | Ivone Leong reviewed gene: TTC8: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Leber congenital amaurosis 15, Retinitis pigmentosa 14, 613843, 600132; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | TTC8 |
Ivone Leong Source NHS GMS was added to TTC8. Mode of inheritance for gene TTC8 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Retinitis pigmentosa 51, 613464; Bardet-Biedl syndrome 8, 615985 for gene: TTC8 |
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| Structural eye disease v0.2 | TTC8 |
Ellen McDonagh gene: TTC8 was added gene: TTC8 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: TTC8 was set to Phenotypes for gene: TTC8 were set to Eye Disorders |
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