Activity

Filter

Cancel
Date Panel Item Activity
4 actions
Structural eye disease v0.76 CRX Nicola Ragge reviewed gene: CRX: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Cone-rod retinal dystrophy-2, Leber congenital amaurosis 7, 120970, 613829; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Structural eye disease v0.38 CRX Ivone Leong reviewed gene: CRX: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Cone-rod retinal dystrophy-2, 120970, Leber congenital amaurosis 7, 613829; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Structural eye disease v0.15 CRX Ivone Leong Source NHS GMS was added to CRX.
Mode of inheritance for gene CRX was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes Leber congenital amaurosis 7, 613829; Cone-rod retinal dystrophy-2, 120970 for gene: CRX
Structural eye disease v0.2 CRX Ellen McDonagh gene: CRX was added
gene: CRX was added to Structural eye disease. Sources: Expert Review Red
Mode of inheritance for gene: CRX was set to
Phenotypes for gene: CRX were set to Eye Disorders