Terminology Service for NFDI4Health
Wagner disease
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http://purl.obolibrary.org/obo/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. [ ]
Term info
Label
Wagner disease
Synonyms
- VCAN-related vitreoretinopathy
- Wagner disease
- Wagner syndrome
- dominant hyaloideoretinal dystrophy of Wagner
- vitreoretinal degeneration, Wagner type
Subsets
ordo_disease
closeMatch
http://identifiers.org/meddra/10063383
exactMatch
http://purl.obolibrary.org/obo/Orphanet_898, https://omim.org/entry/143200, http://identifiers.org/mesh/C536075, http://linkedlifedata.com/resource/umls/id/C1840452, http://identifiers.org/snomedct/232064001
has related synonym
Wagner syndrome 1, erosive vitreoretinopathy, Wagner vitreoretinal Degeneration, Wagner vitreoretinopathy, Wagner syndrome type 1, ERVR, Wagner disease (formerly), hyaloideoretinal Degeneration of Wagner, WGN1, WGVRP
id
MONDO:0007740