{"orpha":324936,"name":"Unclassified autoinflammatory syndrome","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-324936/","orphanet_url":"https://www.orpha.net/en/disease/detail/324936","names":{"fr":{"name":"Syndrome auto-inflammatoire non classé"},"de":{"name":"Autoinflammatorisches Syndrom, unklassifiziertes"},"es":{"name":"Síndrome autoinflamatorio no clasificado"},"it":{"name":"Sindrome autoinfiammatoria non classificata"},"nl":{"name":"Niet-geclassificeerd auto-inflammatoir syndroom"},"pt":{"name":"Síndrome autoinflamatória não classificada"},"pl":{"name":"Niesklasyfikowany zespół autozapalenia"},"cs":{"name":"Neklasifikovaný autoinflamatorní syndrom"},"uk":{"name":"Некласифікований аутозапальний синдром"},"zh":{"name":"未分类的自身炎症综合征"},"tr":{"name":"Sınıflandırılmamış otoinflamatuar sendrom"}},"xrefs":[{"source":"MONDO","code":"17957","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680959","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":476102,"name":"OBSOLETE: Hereditary pediatric Behçet-like disease","status":"inactive"}],"preferential_parent":{"orpha":98023,"name":"Rare systemic or rheumatologic disease"},"parents":[{"orpha":93665,"name":"Autoinflammatory syndrome","classifications":[196]}],"children":[{"orpha":117,"name":"Behçet disease","type":"Disease"},{"orpha":184,"name":"Cherubism","type":"Malformation syndrome"},{"orpha":674762,"name":"Early-onset autoinflammatory syndrome due to A20 haploinsufficiency","type":"Disease"},{"orpha":251307,"name":"Idiopathic recurrent pericarditis","type":"Disease"},{"orpha":324972,"name":"MAGIC syndrome","type":"Disease"},{"orpha":619363,"name":"NOCARH syndrome","type":"Disease"},{"orpha":596759,"name":"RELA haploinsufficiency-associated inflammatory disease","type":"Disease"},{"orpha":723218,"name":"SITRAME Syndrome","type":"Clinical syndrome"},{"orpha":596753,"name":"VEXAS syndrome","type":"Disease"},{"orpha":676125,"name":"X-linked immune dysregulation with inflammatory bowel disease due to ELF4 deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":["Antenatal","Infancy","Neonatal"],"prevalence":[],"phenotypes":null}