|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||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. (Orphanet Rare Disease Ontology, Orphanet_898)|
|Downloads & Tools|
1 genes associated with the Wagner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.