Wagner disease

MONDO:0007740

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.

Also known as: VCAN-related vitreoretinopathy, Wagner disease, Wagner syndrome, dominant hyaloideoretinal dystrophy of Wagner, vitreoretinal degeneration, Wagner type, ERVR, WGN1, WGVRP

22 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by