Wagner disease is a rare hereditary vitreoretinopathy characterized by an anomaleous vitreous associated with myopia, cataract, chorioretinal atrophy, and peripheral tractional or rhegmatogenous retinal detachment. The disease is Wagner disease (MONDO_0007740). Also known as: VCAN-related vitreoretinopathy, Wagner syndrome, dominant hyaloideoretinal dystrophy of Wagner, vitreoretinal degeneration, Wagner type.