{"orpha":519300,"name":"OBSOLETE: Isolated chorioretinal dystrophy","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare predominantly chorioretinal disorder","url":"https://raremap.alftech.space/d/ORPHA-519300/","orphanet_url":"https://www.orpha.net/en/disease/detail/519300","names":{"fr":{"name":"OBSOLETE : Dystrophie choriorétinienne isolée"},"de":{"name":"OBSOLET: Isolierte chorioretinale Dystrophie"},"es":{"name":"OBSOLETO: Distrofia coriorretiniana aislada"},"it":{"name":"OBSOLETO: Distrofia corioretinica isolata"},"nl":{"name":"OBSOLEET: Geïsoleerde chorioretinale dystrofie"},"pt":{"name":"OBSOLETO: Distrofia coriorretiniana isolada"},"pl":{"name":"NIEAKTUALNE: Izolowana dystrofia naczyniówki i siatkówki"},"cs":{"name":"NEAKTUÁLNÍ: Izolovaná chorioretinální dystrofie"},"uk":{"name":"Ізольована хоріоретинальна дистрофія"},"zh":{"name":"孤立性脉络膜视网膜营养不良"},"tr":{"name":"İzole koryoretinal distrofi"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":716290,"name":"Rare predominantly chorioretinal disorder"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}