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Summary Literature (0)
DOID:9719 - neovascular inflammatory vitreoretinopathy

Disease Ontology Definition:A retinal and vitreous disease characterized by ocular inflammation, vascular dropout, large spots of hyperpigmentation, neovascularization of the peripheral and posterior retina, vitreous hemorrhage, and retinal detachment that has_material_basis_in heterozygous mutation in the CAPN5 gene on chromosome 11q13.5.

Synonyms: ADNIV, autosomal dominant neovascular inflammatory vitreoretinopathy, proliferative vitreoretinopathy, Retinitis proliferans

Xenbase Genes : capn5

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0006928 - obsolete proliferative vitreoretinopathy

MIM:
MIM:193235 - VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY; VRNI

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): retinal disease (is_a), vitreous disease (is_a)