An autosomal dominant vitreoretinopathy caused by variants in the CAPN5 gene. Additional features, such as developmental delay and hypotonia, have been reported in some patients. The disease is CAPN5-related vitreoretinopathy (MONDO_0100450). Also known as: ADNIV, CAPN5 vitreoretinopathy, VRNI, autosomal dominant neovascular inflammatory vitreoretinopathy, retinitis proliferans, vitreoretinopathy, neovascular inflammatory, vitreoretinopathy, neovascular inflammatory, autosomal dominant.