{"orpha":716450,"name":"Rare non-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-716450/","orphanet_url":"https://www.orpha.net/en/disease/detail/716450","names":{"fr":{"name":"Vasculopathie rétinienne non-progressive rare"},"de":{"name":"Seltene nicht-progrediente retinale Vaskulopathie"},"es":{"name":"Vasculopatía retiniana no progresiva rara"},"it":{"name":"Vasculopatia retinica rara non progressiva"},"nl":{"name":"Zeldzame niet-progressieve retinale vasculopathie"},"pt":{"name":"Rare non-progressive retinal vasculopathy"},"pl":{"name":"Rzadka niepostępująca waskulopatia siatkówki"},"cs":{"name":"Rare non-progressive retinal vasculopathy"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":519317,"name":"Rare retinal vasculopathy","classifications":[189]}],"children":[{"orpha":648684,"name":"Central retinal artery occlusion","type":"Disease"},{"orpha":353334,"name":"Congenital retinal arteriovenous communication","type":"Morphological anomaly"},{"orpha":284247,"name":"Familial retinal arterial macroaneurysm","type":"Malformation syndrome"},{"orpha":674924,"name":"Isolated retinal racemose hemangioma","type":"Disease"},{"orpha":674930,"name":"Perifoveal exudative vascular anomalous complex","type":"Disease"},{"orpha":71213,"name":"Retinal cavernous hemangioma","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}