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Structural eye disease v0.76 MYO7A Nicola Ragge reviewed gene: MYO7A: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Usher syndrome, type 1B, Deafness, autosomal recessive 2, Deafness, autosomal dominant 11, 276900, 601317; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Structural eye disease v0.48 MYO7A Ivone Leong edited their review of gene: MYO7A: Changed phenotypes: Usher syndrome, type 1B, 276900, Deafness, autosomal recessive 2, Deafness, autosomal dominant 11, 601317
Structural eye disease v0.38 MYO7A Ivone Leong reviewed gene: MYO7A: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Microphthalmia, syndromic 1, 309800; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Structural eye disease v0.15 MYO7A Ivone Leong Source NHS GMS was added to MYO7A.
Mode of inheritance for gene MYO7A was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes Deafness, autosomal recessive 2; Usher syndrome, type 1B, 276900; Deafness, autosomal dominant 11, 601317 for gene: MYO7A
Structural eye disease v0.2 MYO7A Ellen McDonagh gene: MYO7A was added
gene: MYO7A was added to Structural eye disease. Sources: Expert Review Red
Mode of inheritance for gene: MYO7A was set to
Phenotypes for gene: MYO7A were set to Eye Disorders