Preferred Label : Wagner disease;
ICD-11 definition : 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.;
ICD-11 synonym : Vitreoretinal degeneration, Wagner type; Wagner syndrome; Dominant hyaloideoretinal dystrophy of Wagner; VCAN-related vitreoretinopathy;
Origin ID : 780893571;
Automatic exact mappings (from CISMeF team)
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.
