All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01372 WGVRP vitreoretinopathy, Wagner (WGVRP, Wagner syndrome) 143200 4 4 VCAN - -