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| Structural eye disease v0.76 | USH1C | Nicola Ragge reviewed gene: USH1C: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Deafness, autosomal recessive 18A, Usher syndrome type 1C, 602092, 276904; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | USH1C | Ivone Leong edited their review of gene: USH1C: Changed phenotypes: Deafness, autosomal recessive 18A, 602092, Usher syndrome type 1C, 276904 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | USH1C | Ivone Leong reviewed gene: USH1C: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Usher syndrome, type 1G, 606943; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | USH1C |
Ivone Leong Source NHS GMS was added to USH1C. Mode of inheritance for gene USH1C was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Deafness, autosomal recessive 18A, 602092; Usher syndrome type 1C, 276904 for gene: USH1C |
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| Structural eye disease v0.2 | USH1C |
Ellen McDonagh gene: USH1C was added gene: USH1C was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: USH1C was set to Phenotypes for gene: USH1C were set to Eye Disorders |
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