has material basis in germline mutation in VCAN Wagner disease https://www.malacards.org/card/wagner_disease https://www.malacards.org/card/wagner_vitreoretinopathy MESH:C536075 dominant hyaloideoretinal dystrophy of Wagner ERVR vitreoretinal degeneration, Wagner type VCAN-related vitreoretinopathy SCTID:232064001 OMIM:143200 WGN1 hyaloideoretinal Degeneration of Wagner Wagner vitreoretinal Degeneration Orphanet:898 MedDRA:10063383 Wagner disease WGVRP UMLS:C1840452 Wagner syndrome MEDGEN:326741 Wagner disease (formerly) Wagner syndrome type 1 Wagner syndrome 1 erosive vitreoretinopathy GARD:0007871 Wagner vitreoretinopathy 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. icd11.foundation:780893571 vitreoretinal degeneration