Autosomal dominant optic atrophy, classic type (ADOA) is a form of genetic optic atrophy (GOA; see this term), presenting as a symmetric and bilateral decrease in visual acuity, visual field and color vision defects. The disease is Autosomal dominant optic atrophy, classic type (Orphanet_98673, an Orphanet rare-disease nomenclature identifier). Also known as: Autosomal dominant optic atrophy, Kjer type, Kjer disease.