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Retinal disorders v2.298 CNGB3 Arina Puzriakova Phenotypes for gene: CNGB3 were changed from Achromatopsia; Macular degeneration, juvenile; Achromatopsia-3, 262300; Macular degeneration, juvenile, 248200 -3; Stargardt Disease, Recessive; Macular Dystrophy/Degeneration/Stargardt Disease; Achromatopsia-3; Eye Disorders; Achromatopsia, Cone, and Cone-rod Dystrophy to Achromatopsia 3, OMIM:262300; Macular degeneration, juvenile
Retinal disorders v1.159 CNGB3 Gavin Arno reviewed gene: CNGB3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Retinal disorders v1.137 CNGB3 Ivone Leong Source NHS GMS was added to CNGB3.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Retinal disorders CNGB3 Ellen McDonagh edited their review of CNGB3
Retinal disorders CNGB3 BRIDGE consortium reviewed CNGB3