{"orpha":716299,"name":"Rare disorder with non-progressive predominantly chorioretinal disorder as a major feature","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Rare syndromic non-progressive predominantly chorioretinal disorder"],"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-716299/","orphanet_url":"https://www.orpha.net/en/disease/detail/716299","names":{"fr":{"name":"Maladie rare avec atteinte non-progressive prédominante de la choroïde et de la rétine comme manifestation majeure","synonyms":["Maladie rare syndromique avec atteinte non-progressive prédominante de la rétine et de la choroïde"]},"de":{"name":"Seltene Störung mit nicht-progredienter chorioretinaler Störung als Hauptmerkmal"},"es":{"name":"Trastorno raro con afectación predominantemente coriorretiniana no progresiva como característica principal","synonyms":["Trastorno raro predominantemente coriorretiniano no progresivo sindrómico"]},"it":{"name":"Malattia rara con anomalia a predominanza corioretinica come caratteristica principale","synonyms":["Malattia rara sindromica a predominanza corioretinica non progressiva"]},"nl":{"name":"Zeldzame aandoening met niet-progressieve aandoening van voornamelijk choroidea en/of retina als een hoofdkenmerk","synonyms":["Zeldzame aandoening met niet-progressieve aandoening van voornamelijk vaatvlies en/of netvlies als een hoofdkenmerk","Zeldzame aandoening met niet-progressieve overwegend chorioretinale aandoening als een hoofdkenmerk","Zeldzame syndromale niet-progressieve aandoening van voornamelijk choroidea en/of retina","Zeldzame syndromale niet-progressieve aandoening van voornamelijk vaatvlies en/of netvlies","Zeldzame syndromale niet-progressieve overwegend chorioretinale aandoening"]},"pt":{"name":"Rare disorder with non-progressive predominantly chorioretinal disorder as a major feature"},"pl":{"name":"Rzadkie zaburzenie z niepostępującą chorobą dotyczącą głównie naczyniówki i siatkówki jako dominującą cechą","synonyms":["Rare syndromic non-progressive predominantly chorioretinal disorder"]},"cs":{"name":"Rare disorder with non-progressive predominantly chorioretinal disorder as a major feature","synonyms":["Rare syndromic non-progressive predominantly chorioretinal disorder"]}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":717308,"name":"Rare genetic non-progressive predominantly chorioretinal disorder","classifications":[156]},{"orpha":716293,"name":"Rare non-progressive predominantly chorioretinal disorder","classifications":[189]}],"children":[{"orpha":50,"name":"Aicardi syndrome","type":"Disease"},{"orpha":1433,"name":"Choroidal atrophy-alopecia syndrome","type":"Malformation syndrome"},{"orpha":1884,"name":"Ectopia lentis-chorioretinal dystrophy-myopia syndrome","type":"Disease"},{"orpha":369970,"name":"Microcornea-myopic chorioretinal atrophy-telecanthus syndrome","type":"Disease"},{"orpha":139450,"name":"Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}