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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
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