{"orpha":619238,"name":"Rare hereditary autoinflammatory disease","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-619238/","orphanet_url":"https://www.orpha.net/en/disease/detail/619238","names":{"fr":{"name":"Maladie auto-inflammatoire héréditaire rare"},"de":{"name":"Seltene hereditäre autoinflammatorische Krankheit"},"es":{"name":"Enfermedad autoinflamatoria hereditaria rara"},"it":{"name":"Malattia autoinfiammatoria ereditaria rara"},"nl":{"name":"Zeldzame hereditaire auto-inflammatoire aandoening","synonyms":["Zeldzame erfelijke auto-inflammatoire aandoening"]},"pt":{"name":"Doença autoinflamatória hereditária rara"},"pl":{"name":"Rzadka dziedziczna choroba autozapalna"},"cs":{"name":"Vzácné dědičné autoinflamatorní onemocnění"},"uk":{"name":"Рідкісне спадкове аутозапальне захворювання"}},"xrefs":[{"source":"UMLS","code":"C5816810","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98023,"name":"Rare systemic or rheumatologic disease"},"parents":[{"orpha":271870,"name":"Rare genetic systemic or rheumatologic disease","classifications":[156]}],"children":[{"orpha":90340,"name":"Blau syndrome","type":"Disease"},{"orpha":184,"name":"Cherubism","type":"Malformation syndrome"},{"orpha":404546,"name":"DITRA","type":"Disease"},{"orpha":674762,"name":"Early-onset autoinflammatory syndrome due to A20 haploinsufficiency","type":"Disease"},{"orpha":652510,"name":"Genetic autoinflammatory syndrome with acne and/or hidradenitis suppurativa","type":"Clinical group"},{"orpha":324924,"name":"Hereditary periodic fever syndrome","type":"Category"},{"orpha":251523,"name":"Hyperzincemia and hypercalprotectinemia","type":"Disease"},{"orpha":77297,"name":"Majeed syndrome","type":"Disease"},{"orpha":324933,"name":"Mixed autoinflammatory and autoimmune syndrome","type":"Category"},{"orpha":619363,"name":"NOCARH syndrome","type":"Disease"},{"orpha":294023,"name":"Neonatal erythroderma-autoinflammation-inflammatory bowel disease syndrome","type":"Disease"},{"orpha":48104,"name":"Pyoderma gangrenosum","type":"Disease"},{"orpha":210115,"name":"Sterile multifocal osteomyelitis with periostitis and pustulosis","type":"Disease"},{"orpha":3243,"name":"Sweet syndrome","type":"Disease"},{"orpha":477647,"name":"Type 1 interferonopathy","type":"Category"},{"orpha":676125,"name":"X-linked immune dysregulation with inflammatory bowel disease due to ELF4 deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}