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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 |
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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 |