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| Structural eye disease v0.76 | MERTK | Nicola Ragge reviewed gene: MERTK: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinitis pigmentosa 38, 613862; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.47 | MERTK | Ivone Leong edited their review of gene: MERTK: Changed phenotypes: Retinitis pigmentosa 38, 613862 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | MERTK | Ivone Leong reviewed gene: MERTK: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Charcot-Marie-Tooth disease, type 2A2, 609260; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | MERTK |
Ivone Leong Source NHS GMS was added to MERTK. Mode of inheritance for gene MERTK was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Retinitis pigmentosa 38, 613862 for gene: MERTK |
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| Structural eye disease v0.2 | MERTK |
Ellen McDonagh gene: MERTK was added gene: MERTK was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: MERTK was set to Phenotypes for gene: MERTK were set to Eye Disorders |
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