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| Structural eye disease v0.76 | SDCCAG8 | Nicola Ragge reviewed gene: SDCCAG8: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Senior-Loken syndrome 7, Bardet-Biedl syndrome 16, 613615, 615993; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | SDCCAG8 | Ivone Leong edited their review of gene: SDCCAG8: Changed phenotypes: Senior-Loken syndrome 7, 613615, Bardet-Biedl syndrome 16, 615993 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | SDCCAG8 | Ivone Leong reviewed gene: SDCCAG8: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 35, 610282, Cone-rod dystrophy 10, 610283; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | SDCCAG8 |
Ivone Leong Source NHS GMS was added to SDCCAG8. Mode of inheritance for gene SDCCAG8 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Bardet-Biedl syndrome 16, 615993; Senior-Loken syndrome 7, 613615 for gene: SDCCAG8 |
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| Structural eye disease v0.2 | SDCCAG8 |
Ellen McDonagh gene: SDCCAG8 was added gene: SDCCAG8 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: SDCCAG8 was set to Phenotypes for gene: SDCCAG8 were set to Eye Disorders |
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