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| Structural eye disease v0.76 | LCA5 | Nicola Ragge reviewed gene: LCA5: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Leber congenital amaurosis 5, 604537; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | LCA5 | Ivone Leong reviewed gene: LCA5: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Leber congenital amaurosis 5, 604537; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | LCA5 |
Ivone Leong Source NHS GMS was added to LCA5. Mode of inheritance for gene LCA5 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Leber congenital amaurosis 5, 604537 for gene: LCA5 |
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| Structural eye disease v0.2 | LCA5 |
Ellen McDonagh gene: LCA5 was added gene: LCA5 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: LCA5 was set to Phenotypes for gene: LCA5 were set to Eye Disorders |
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