{"orpha":716198,"name":"Rare paraneoplastic choroidal disorder","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-716198/","orphanet_url":"https://www.orpha.net/en/disease/detail/716198","names":{"fr":{"name":"Maladie choroïdienne paranéoplasique rare"},"de":{"name":"Seltene paraneoplastische choroidale Krankheit"},"es":{"name":"Trastorno coroideo paraneoplásico raro"},"it":{"name":"Malattia paraneoplastica rara della coroide"},"nl":{"name":"Zeldzame paraneoplastische aandoening van choroidea","synonyms":["Zeldzame paraneoplastische aandoening van vaatvlies","Zeldzame paraneoplastische choroïdale aandoening"]},"pt":{"name":"Rare paraneoplastic choroidal disorder"},"pl":{"name":"Rzadkie paranowotworowe zaburzenie naczyniówki"},"cs":{"name":"Rare paraneoplastic choroidal disorder"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":519309,"name":"Rare choroidal disorder","classifications":[189]},{"orpha":101950,"name":"Rare eye tumor","classifications":[189,202]}],"children":[{"orpha":674968,"name":"Bilateral diffuse uveal melanocytic proliferation disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}