{"orpha":717314,"name":"Rare genetic progressive 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-717314/","orphanet_url":"https://www.orpha.net/en/disease/detail/717314","names":{"fr":{"name":"Maladie génétique rare avec atteinte progressive prédominante de la choroïde et de la rétine"},"de":{"name":"Seltene genetische progrediente vorwiegend chorioretinale Störung"},"es":{"name":"Trastorno genético raro predominantemente coriorretiniano progresivo"},"it":{"name":"Malattia genetica rara progressiva a predominanza corioretinica"},"nl":{"name":"Zeldzame genetische progressieve aandoening van voornamelijk choroidea en/of retina","synonyms":["Zeldzame genetische progressieve aandoening van voornamelijk vaatvlies en/of netvlies","Zeldzame genetische progressieve overwegend chorioretinale aandoening"]},"pt":{"name":"Rare genetic progressive predominantly chorioretinal disorder"},"pl":{"name":"Rzadkie genetycznie uwarunkowane postępujące zaburzenie dotyczące głównie naczyniówki i siatkówki"},"cs":{"name":"Rare genetic progressive predominantly chorioretinal disorder"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":717257,"name":"Rare genetic predominantly chorioretinal disorder","classifications":[156]}],"children":[{"orpha":716342,"name":"Rare disorder with progressive predominantly chorioretinal disorder as a major feature","type":"Category"},{"orpha":717317,"name":"Rare genetic isolated progressive predominantly chorioretinal disorder","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}