{"orpha":717345,"name":"Rare genetic isolated progressive retinal vasculopathy","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-717345/","orphanet_url":"https://www.orpha.net/en/disease/detail/717345","names":{"fr":{"name":"Vasculopathie génétique rare rétinienne isolée progressive"},"de":{"name":"Seltene genetische isolierte progressive retinale Vaskulopathie"},"es":{"name":"Vasculopatía retiniana progresiva aislada genética rara"},"it":{"name":"Vasculopatia retinica genetica rara isolata progressiva"},"nl":{"name":"Zeldzame genetische geïsoleerde progressieve retinale vasculopathie"},"pt":{"name":"Rare genetic isolated progressive retinal vasculopathy"},"pl":{"name":"Rzadka genetycznie uwarunkowana izolowana postępująca waskulopatia siatkówki"},"cs":{"name":"Rare genetic isolated progressive retinal vasculopathy"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":717342,"name":"Rare genetic progressive retinal vasculopathy","classifications":[156]}],"children":[{"orpha":329211,"name":"Autosomal dominant neovascular inflammatory vitreoretinopathy","type":"Disease"},{"orpha":891,"name":"Familial exudative vitreoretinopathy","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}