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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: Retinitis proliferans, ADNIV, proliferative vitreoretinopathy, autosomal dominant neovascular inflammatory vitreoretinopathy
Echinobase Genes
:
capn5
| 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)