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| Structural eye disease v0.76 | CLRN1 | Nicola Ragge reviewed gene: CLRN1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Usher syndrome, type 3A, Retinitis pigmentosa 61, 276902, 614180; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | CLRN1 | Ivone Leong reviewed gene: CLRN1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Usher syndrome, type 3A, 276902, Retinitis pigmentosa 61, 614180; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | CLRN1 |
Ivone Leong Source NHS GMS was added to CLRN1. Mode of inheritance for gene CLRN1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Usher syndrome, type 3A, 276902; Retinitis pigmentosa 61, 614180 for gene: CLRN1 |
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| Structural eye disease v0.2 | CLRN1 |
Ellen McDonagh gene: CLRN1 was added gene: CLRN1 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: CLRN1 was set to Phenotypes for gene: CLRN1 were set to Eye Disorders |
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