Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/143200 http://purl.bioontology.org/ontology/OMIM/143200
Preferred Name	WAGNER VITREORETINOPATHY
Synonyms	ERVR HYALOIDEORETINAL DEGENERATION OF WAGNER WAGNER VITREORETINAL DEGENERATION EROSIVE VITREORETINOPATHY WGVRP WAGNER SYNDROME 1 WGN1
Type	http://www.w3.org/2002/07/owl#Class

altLabel	ERVR HYALOIDEORETINAL DEGENERATION OF WAGNER WAGNER VITREORETINAL DEGENERATION EROSIVE VITREORETINOPATHY WGVRP WAGNER SYNDROME 1 WGN1 See more See less
prefLabel	WAGNER VITREORETINOPATHY
Gene Symbol	CSPG2 ERVR WGN VCAN WGN1
Scope Statement	Caused by mutation in the chondroitin sulfate proteoglycan-2 gene (CSPG2, 118661.0001) [MOLECULAR BASIS] Progressive clinical course with onset in childhood [MISCELLANEOUS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU002188 http://purl.bioontology.org/ontology/OMIM/MTHU017823 http://purl.bioontology.org/ontology/OMIM/MTHU017820 http://purl.bioontology.org/ontology/OMIM/MTHU018963 http://purl.bioontology.org/ontology/OMIM/MTHU017814 http://purl.bioontology.org/ontology/OMIM/MTHU004637 http://purl.bioontology.org/ontology/OMIM/MTHU031018 http://purl.bioontology.org/ontology/OMIM/MTHU004639 http://purl.bioontology.org/ontology/OMIM/MTHU017819 http://purl.bioontology.org/ontology/OMIM/MTHU031017 http://purl.bioontology.org/ontology/OMIM/MTHU036360 http://purl.bioontology.org/ontology/OMIM/MTHU067197 http://purl.bioontology.org/ontology/OMIM/MTHU017821 See more See less
tui	T047
Gene Locus	5q12-q14
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	143200
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000018
cui	C1840452
OMIM Entry Type	3
OMIM MimType Value	pound

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