{"orpha":567556,"name":"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-567556/","orphanet_url":"https://www.orpha.net/en/disease/detail/567556","names":{"fr":{"name":"Maladie systémique d'origine génétique avec une glomérulopathie comme manifestation majeure"},"de":{"name":"Genetisch bedingte systemische Krankheit mit Glomerulopathie als Hauptmerkmal"},"es":{"name":"Enfermedad sistémica genética con glomerulopatía como característica principal"},"it":{"name":"Malattia sistemica genetica a prevalente espressione glomerulopatica"},"nl":{"name":"Genetische systemische ziekte met glomerulopathie als hoofdkenmerk"},"pt":{"name":"Glomerulopatia como característica principal em doença sistémica genética"},"pl":{"name":"Genetyczna choroba wieloukładowa z glomerulopatią jako głównym objawem"},"cs":{"name":"Genetické systémové onemocnění s glomerulopatií jako hlavním příznakem"},"uk":{"name":"Генетично обумовлене системне захворювання з гломерулопатією як основною ознакою"},"zh":{"name":"以肾小球病变为主要特征的遗传性系统性疾病"},"tr":{"name":"Esas klinik özelliği glomerülopati olan genetik sistemik hastalık"}},"xrefs":[{"source":"UMLS","code":"C5681295","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98023,"name":"Rare systemic or rheumatologic disease"},"parents":[{"orpha":183586,"name":"Genetic glomerular disease","classifications":[156]},{"orpha":567554,"name":"Systemic disease with glomerulopathy as a major feature","classifications":[188,233]}],"children":[{"orpha":444092,"name":"Autoimmune interstitial lung disease-arthritis syndrome","type":"Disease"},{"orpha":342,"name":"Familial Mediterranean fever","type":"Disease"},{"orpha":85450,"name":"Hereditary amyloidosis with primary renal involvement","type":"Disease"},{"orpha":36412,"name":"Hypocomplementemic urticarial vasculitis","type":"Disease"},{"orpha":575,"name":"Muckle-Wells syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}