{"orpha":520817,"name":"OBSOLETE: Isolated inherited retinal disorder","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 genetic retinal disorder","url":"https://raremap.alftech.space/d/ORPHA-520817/","orphanet_url":"https://www.orpha.net/en/disease/detail/520817","names":{"fr":{"name":"OBSOLETE : Maladie rétinienne héréditaire isolée"},"de":{"name":"OBSOLET: Isolierte hereditäre retinale Störung"},"es":{"name":"OBSOLETO: Trastorno retiniano hereditario aislado"},"it":{"name":"OBSOLETO: Patologia retinica ereditaria isolata"},"nl":{"name":"OBSOLEET: Geïsoleerde erfelijke aandoening van retina","synonyms":["NIET ZELDZAME ZIEKTE IN EUROPA: Geïsoleerde erfelijke aandoening van netvlies"]},"pt":{"name":"OBSOLETO: Doença retiniana hereditária isolada"},"pl":{"name":"NIEAKTUALNE: Izolowana wrodzona choroba siatkówki"},"cs":{"name":"NEAKTUÁLNÍ: Izolovaná dědičná porucha sítnice"},"uk":{"name":"Ізольоване спадкове захворювання сітківки"},"zh":{"name":"孤立性遗传性视网膜疾病"},"tr":{"name":"İzole kalıtsal retina bozukluğu"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":522572,"name":"Rare genetic retinal disorder"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}