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| Structural eye disease v0.76 | LRAT | Nicola Ragge reviewed gene: LRAT: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Leber congenital amaurosis 14, 613341; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | LRAT | Ivone Leong reviewed gene: LRAT: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Leber congenital amaurosis 14, 613341; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | LRAT |
Ivone Leong Source NHS GMS was added to LRAT. Mode of inheritance for gene LRAT was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Leber congenital amaurosis 14, 613341 for gene: LRAT |
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| Structural eye disease v0.2 | LRAT |
Ellen McDonagh gene: LRAT was added gene: LRAT was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: LRAT was set to Phenotypes for gene: LRAT were set to Eye Disorders |
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