{"orpha":716290,"name":"Rare predominantly chorioretinal 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-716290/","orphanet_url":"https://www.orpha.net/en/disease/detail/716290","names":{"fr":{"name":"Maladie avec atteinte prédominante de la choroïde et de la rétine rare"},"de":{"name":"Seltene chorioretinale Störung"},"es":{"name":"Trastorno raro predominantemente coriorretiniano"},"it":{"name":"Malattia rara a predominanza corioretinica"},"nl":{"name":"Zeldzame aandoening van voornamelijk choroidea en/of retina","synonyms":["Zeldzame aandoening van voornamelijk vaatvlies en/of netvlies","Zeldzame overwegend chorioretinale aandoening"]},"pt":{"name":"Rare predominantly chorioretinal disorder"},"pl":{"name":"Rzadkie zaburzenie dotyczące głównie naczyniówki i siatkówki"},"cs":{"name":"Rare predominantly chorioretinal disorder"}},"xrefs":[],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":519300,"name":"OBSOLETE: Isolated chorioretinal dystrophy","status":"inactive"},{"type":"Referred to","orpha":519321,"name":"OBSOLETE: Syndromic chorioretinal dystrophy","status":"inactive"}],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":519315,"name":"Rare retinal disorder","classifications":[189]}],"children":[{"orpha":716293,"name":"Rare non-progressive predominantly chorioretinal disorder","type":"Category"},{"orpha":716304,"name":"Rare progressive predominantly chorioretinal disorder","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}