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| Structural eye disease v0.76 | ZNF513 | Nicola Ragge reviewed gene: ZNF513: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 58, 613617; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | ZNF513 | Ivone Leong edited their review of gene: ZNF513: Changed phenotypes: Retinitis pigmentosa 58, 613617 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | ZNF513 | Ivone Leong reviewed gene: ZNF513: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Microcornea, myopic chorioretinal atrophy, and telecanthus, 615458; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | ZNF513 |
Ivone Leong Source NHS GMS was added to ZNF513. Mode of inheritance for gene ZNF513 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Retinitis pigmentosa 58, 613617 for gene: ZNF513 |
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| Structural eye disease v0.2 | ZNF513 |
Ellen McDonagh gene: ZNF513 was added gene: ZNF513 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: ZNF513 was set to Phenotypes for gene: ZNF513 were set to Eye Disorders |
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