{"orpha":716296,"name":"Rare 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-716296/","orphanet_url":"https://www.orpha.net/en/disease/detail/716296","names":{"fr":{"name":"Maladie rare isolée avec atteinte non-progressive prédominante de la choroïde et de la rétine"},"de":{"name":"Seltene isolierte nicht-progrediente chorioretinale Störung"},"es":{"name":"Trastorno raro predominantemente coriorretiniano no progresivo aislado"},"it":{"name":"Malattia rara isolata a predominanza corioretinica"},"nl":{"name":"Zeldzame geïsoleerde niet-progressieve aandoening van voornamelijk choroidea en/of retina","synonyms":["Zeldzame geïsoleerde niet-progressieve aandoening van voornamelijk vaatvlies en/of netvlies","Zeldzame geïsoleerde niet-progressieve overwegend chorioretinale aandoening"]},"pt":{"name":"Rare isolated non-progressive predominantly chorioretinal disorder"},"pl":{"name":"Rzadkie izolowane niepostępujące zaburzenie dotyczące głównie naczyniówki i siatkówki"},"cs":{"name":"Rare isolated non-progressive predominantly chorioretinal disorder"}},"xrefs":[],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97966,"name":"Rare ophthalmic disorder"},"parents":[{"orpha":716293,"name":"Rare non-progressive predominantly chorioretinal disorder","classifications":[189]}],"children":[{"orpha":98942,"name":"Coloboma of choroid and retina","type":"Morphological anomaly"},{"orpha":715862,"name":"Melanocytoma of the optic disc and optic nerve","type":"Disease"},{"orpha":674953,"name":"Multiple evanescent white dot syndrome","type":"Disease"},{"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}