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Summary Literature (0)
MIM:193235 - VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY; VRNI

Xenbase Genes: capn5

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0006928 - proliferative vitreoretinopathy
MONDO:0008664 - obsolete autosomal dominant neovascular inflammatory vitreoretinopathy
MONDO:0100450 - CAPN5-related vitreoretinopathy

Disease Ontology (DO):
DOID:9719 - neovascular inflammatory vitreoretinopathy