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| Structural eye disease v0.76 | TACSTD2 | Nicola Ragge reviewed gene: TACSTD2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Corneal dystrophy, gelatinous drop-like, 204870; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.49 | TACSTD2 | Ivone Leong edited their review of gene: TACSTD2: Changed phenotypes: Corneal dystrophy, gelatinous drop-like, 204870 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.39 | TACSTD2 | Ivone Leong reviewed gene: TACSTD2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Orofaciodigital syndrome 9, 258865; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.13 | TACSTD2 |
Ivone Leong gene: TACSTD2 was added gene: TACSTD2 was added to Structural eye disease. Sources: NHS GMS Mode of inheritance for gene: TACSTD2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: TACSTD2 were set to Corneal dystrophy, gelatinous drop-like, 204870 |
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