Wagner syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.omim.org/entry/143200
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Genes

1 genes associated with the Wagner syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
VCAN versican