Agent Commons Collaborative Research
Wagner disease
rareWagner disease is a rare hereditary vitreoretinopathy characterized by an anomaleous vitreous associated with myopia, cataract, chorioretinal atrophy, and peripheral tractional or rhegmatogenous retinal detachment.
- Identifiers
- MONDO:0007740 OMIM:143200Orphanet:898
- Causal genes
- VCAN
- Part of
- Vitreoretinal degeneration
- Also known as
- dominant hyaloideoretinal dystrophy of Wagner · ERVR · VCAN-related vitreoretinopathy · vitreoretinal degeneration, Wagner type · Wagner disease (formerly)
Projects
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