{"orpha":567558,"name":"Non-genetic systemic disease with glomerulopathy as a major feature","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-567558/","orphanet_url":"https://www.orpha.net/en/disease/detail/567558","names":{"fr":{"name":"Maladie systémique non génétique avec une glomérulopathie comme manifestation majeure"},"de":{"name":"Nicht genetisch bedingte systemische Krankheit mit Glomerulopathie als Hauptmerkmal"},"es":{"name":"Enfermedad sistémica no genética con glomerulopatía como característica principal"},"it":{"name":"Malattia sistemica non genetica a prevalente espressione glomerulopatica"},"nl":{"name":"Niet-genetische systemische ziekte met glomerulopathie als hoofdkenmerk"},"pt":{"name":"Glomerulopatia como característica principal em doença sistémica não-genética"},"pl":{"name":"Niegenetyczna choroba układowa z glomerulopatią jako głównym objawem"},"cs":{"name":"Negenetické systémové onemocnění s glomerulopatií jako hlavním příznakem"},"uk":{"name":"Системне захворювання з гломерулопатією як основною ознакою без генетичного дефекту"},"zh":{"name":"以肾小球病变为主要特征的非遗传性系统性疾病"},"tr":{"name":"Esas klinik özelliği glomerülopati olan genetik olmayan sistemik hastalık"}},"xrefs":[{"source":"UMLS","code":"C5681296","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98023,"name":"Rare systemic or rheumatologic disease"},"parents":[{"orpha":567554,"name":"Systemic disease with glomerulopathy as a major feature","classifications":[188,233]}],"children":[{"orpha":85445,"name":"AA amyloidosis","type":"Disease"},{"orpha":439232,"name":"AApoAIV amyloidosis","type":"Disease"},{"orpha":442582,"name":"AH amyloidosis","type":"Disease"},{"orpha":85443,"name":"AL amyloidosis","type":"Disease"},{"orpha":829,"name":"Adult-onset Still disease","type":"Disease"},{"orpha":117,"name":"Behçet disease","type":"Disease"},{"orpha":221,"name":"Dermatomyositis","type":"Disease"},{"orpha":449395,"name":"IgG4-related kidney disease","type":"Clinical subtype"},{"orpha":93672,"name":"Juvenile dermatomyositis","type":"Disease"},{"orpha":93568,"name":"Juvenile polymyositis","type":"Disease"},{"orpha":809,"name":"Mixed connective tissue disease","type":"Disease"},{"orpha":86861,"name":"Non-amyloid monoclonal immunoglobulin deposition disease","type":"Disease"},{"orpha":732,"name":"Polymyositis","type":"Disease"},{"orpha":779,"name":"Reynolds syndrome","type":"Disease"},{"orpha":797,"name":"Sarcoidosis","type":"Disease"},{"orpha":90291,"name":"Systemic sclerosis","type":"Disease"},{"orpha":567560,"name":"Systemic vasculitis associated with glomerulopathy","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}