{"orpha":93217,"name":"OBSOLETE: Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis","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-93217/","orphanet_url":"https://www.orpha.net/en/disease/detail/93217","names":{"fr":{"name":"OBSOLETE : Syndrome néphrotique idiopathique familial corticorésistant avec sclérose mésangiale diffuse"},"de":{"name":"OBSOLET: Nephrotisches Syndrom, familiäres idiopathisches steroid-resistentes, mit diffuser mesangialer Sklerose"},"es":{"name":"OBSOLETO: Síndrome nefrótico familiar idiopático resistente a esteroides con esclerosis mesangial difusa"},"it":{"name":"OBSOLETO: Sindrome nefrosica idiopatica steroido-resistente con sclerosi mesangiale diffusa, forma familiare"},"nl":{"name":"OBSOLEET: Familiaal idiopathisch steroïderesistent nefrotisch syndroom met diffuse mesangiale sclerose"},"pt":{"name":"OBSOLETO: Síndrome nefrótica corticorresistente idiopática familiar com esclerose mesangial difusa"},"pl":{"name":"NIEAKTUALNE: Rodzinny steroidooporny idiopatyczny zespól nerczycowy z rozlanym stwardnieniem mezangium"},"cs":{"name":"NEAKTUÁLNÍ: Familiární idiopatický nefrotický syndrom rezistentní na steroidy s difuzní sklerózou mesangia"},"uk":{"name":"ЗАСТАРІЛО: Сімейний ідіопатичний стероїдорезистентний нефротичний синдром з дифузним мезангіальним склерозом"},"zh":{"name":"弃用：家族性激素敏感型原发性肾病综合征伴弥漫性系膜硬化"},"tr":{"name":"Eski adı: Yaygın mezangial skleroz ile seyreden ailesel 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}