{"orpha":717311,"name":"Rare genetic isolated non-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-717311/","orphanet_url":"https://www.orpha.net/en/disease/detail/717311","names":{"fr":{"name":"Maladie génétique rare isolée avec atteinte non-progressive prédominante de la choroïde et de la rétine"},"de":{"name":"Seltene genetische isolierte nicht-progrediente chorioretinale Störung"},"es":{"name":"Trastorno genético raro predominantemente coriorretiniano no progresivo aislado"},"it":{"name":"Malattia genetica rara non progressiva a predominanza corioretinica isolata"},"nl":{"name":"Zeldzame genetische geïsoleerde niet-progressieve aandoening van voornamelijk choroidea en/of retina","synonyms":["Zeldzame genetische geïsoleerde niet-progressieve aandoening van voornamelijk vaatvlies en/of netvlies","Zeldzame genetische geïsoleerde niet-progressieve overwegend chorioretinale aandoening"]},"pt":{"name":"Rare genetic isolated non-progressive predominantly chorioretinal disorder"},"pl":{"name":"Rzadkie genetycznie uwarunkowane izolowane niepostępujące zaburzenie dotyczące głównie naczyniówki i siatkówki"},"cs":{"name":"Rare genetic isolated 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]}],"children":[{"orpha":98942,"name":"Coloboma of choroid and retina","type":"Morphological anomaly"},{"orpha":75327,"name":"North Carolina macular dystrophy","type":"Disease"},{"orpha":251295,"name":"Pigmented paravenous retinochoroidal atrophy","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}