All diseases

OMIM ID
143200
OMIM term:
WAGNER SYNDROME 1; WGN1
Alternative terms:
WAGNER VITREORETINAL DEGENERATION
HYALOIDEORETINAL DEGENERATION OF WAGNER
EROSIVE VITREORETINOPATHY; ERVR
(∗) Location:
5q14.2-q14.3  
(†) Associated OMIM genes:
VCAN  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/il7dtbct