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| Structural eye disease v0.76 | UNC119 | Nicola Ragge reviewed gene: UNC119: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Cone-rod dystrophy, Immunodeficiency 13, , 615518; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.48 | UNC119 | Ivone Leong edited their review of gene: UNC119: Changed phenotypes: Cone-rod dystrophy, Immunodeficiency 13, 615518 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | UNC119 | Ivone Leong reviewed gene: UNC119: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Deafness, autosomal recessive 18A, 602092, Usher syndrome type 1C, 276904; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | UNC119 |
Ivone Leong Source NHS GMS was added to UNC119. Mode of inheritance for gene UNC119 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Cone-rod dystrophy; Immunodeficiency 13, 615518 for gene: UNC119 |
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| Structural eye disease v0.2 | UNC119 |
Ellen McDonagh gene: UNC119 was added gene: UNC119 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: UNC119 was set to Phenotypes for gene: UNC119 were set to Eye Disorders |
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