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| Structural eye disease v0.76 | CHST6 | Nicola Ragge reviewed gene: CHST6: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Macular corneal dystrophy, 217800; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.49 | CHST6 | Ivone Leong edited their review of gene: CHST6: Changed phenotypes: Macular corneal dystrophy, 217800 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.39 | CHST6 | Ivone Leong reviewed gene: CHST6: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Knobloch syndrome, type 1, 267750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.13 | CHST6 |
Ivone Leong gene: CHST6 was added gene: CHST6 was added to Structural eye disease. Sources: NHS GMS Mode of inheritance for gene: CHST6 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: CHST6 were set to Macular corneal dystrophy, 217800 |
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