{"orpha":93221,"name":"OBSOLETE: Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes","type":"Histopathological subtype","group":"Subtype of disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Genetic steroid-resistant nephrotic syndrome","url":"https://raremap.alftech.space/d/ORPHA-93221/","orphanet_url":"https://www.orpha.net/en/disease/detail/93221","names":{"fr":{"name":"OBSOLETE : Syndrome néphrotique idiopathique sporadique corticorésistant à lésions glomérulaires minimes","synonyms":["OBSOLETE : Syndrome néphrotique idiopathique sporadique cortico-résistant à LGM","OBSOLETE : Syndrome néphrotique idiopathique sporadique corticorésistant à LGM"]},"de":{"name":"OBSOLET: Nephrotisches Syndrom, idiopathisches steroid-resistentes, mit glomerulärer Minimalläsion, sporadische Form"},"es":{"name":"OBSOLETO: Síndrome nefrótico esporádico idiopático resistente a esteroides con cambios mínimos"},"it":{"name":"OBSOLETO: Sindrome nefrosica idiopatica steroido-resistente con alterazioni minime, forma sporadica"},"nl":{"name":"OBSOLEET: Sporadisch idiopathisch steroïderesistent nefrotisch syndroom met minimale verandering"},"pt":{"name":"OBSOLETO: Síndrome nefrótica corticorresistente idiopática esporádica com alterações mínimas"},"pl":{"name":"NIEAKTUALNE: Sporadyczny steroidooporny idiopatyczny zespól nerczycowy z minimalnymi zmianami"},"cs":{"name":"NEAKTUÁLNÍ: Sporadický idiopatický nefrotický syndrom rezistentní na steroidy s minimálními změnami"},"uk":{"name":"ЗАСТАРІЛО: Спорадичний ідіопатичний стероїдорезистентний нефротичний синдром з мінімальними змінами"},"zh":{"name":"弃用：散发性激素敏感型原发性肾病综合征伴微小病变"},"tr":{"name":"Eski adı: Minimal değişiklik ile seyreden sporadik idiyopatik steroide dirençli nefrotik sendrom"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":656,"name":"Hereditary steroid-resistant nephrotic syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}