Human genes for neovascular inflammatory vitreoretinopathy
Neovascular inflammatory vitreoretinopathy [DOID:9719]
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 CAPN5 on chromosome 11q13.5.
Synonyms: neovascular inflammatory vitreoretinopathy, DOID:9719, neovascular inflammatory vitreoretinopathies, ADNIV, autosomal dominant neovascular inflammatory vitreoretinopathy ...
Linkouts: OMIM