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Structural eye disease v0.76 | ADGRV1 | Nicola Ragge reviewed gene: ADGRV1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Usher syndrome, type 2C, 605472; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.38 | ADGRV1 | Ivone Leong reviewed gene: ADGRV1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Usher syndrome, type 2C, 605472; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.15 | ADGRV1 |
Ivone Leong Source NHS GMS was added to ADGRV1. Mode of inheritance for gene ADGRV1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Usher syndrome, type 2C, 605472 for gene: ADGRV1 |
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Structural eye disease v0.2 | ADGRV1 |
Ellen McDonagh gene: ADGRV1 was added gene: ADGRV1 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: ADGRV1 was set to Phenotypes for gene: ADGRV1 were set to Eye Disorders |