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Structural eye disease v0.76 | WFS1 | Nicola Ragge reviewed gene: WFS1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Wolfram syndrome, Wolfram-like syndrome, autosomal dominant, ?Cataract 41, 222300, 614296, 116400; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.48 | WFS1 | Ivone Leong edited their review of gene: WFS1: Changed phenotypes: Wolfram syndrome, 222300, Wolfram-like syndrome, autosomal dominant, 614296, ?Cataract 41, 116400 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.38 | WFS1 | Ivone Leong reviewed gene: WFS1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Usher syndrome, type 2D, 611383; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.15 | WFS1 |
Ivone Leong Source NHS GMS was added to WFS1. Mode of inheritance for gene WFS1 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Added phenotypes Wolfram-like syndrome, autosomal dominant, 614296; Wolfram syndrome, 222300; ?Cataract 41, 116400 for gene: WFS1 |
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Structural eye disease v0.2 | WFS1 |
Ellen McDonagh gene: WFS1 was added gene: WFS1 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: WFS1 was set to Phenotypes for gene: WFS1 were set to Eye Disorders |