{"orpha":324942,"name":"Pyogenic autoinflammatory syndrome of childhood","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-324942/","orphanet_url":"https://www.orpha.net/en/disease/detail/324942","names":{"fr":{"name":"Syndrome auto-inflammatoire pyogène de l'enfant"},"de":{"name":"Autoinflammatorisches Syndrom, pyogenes, der Kindheit"},"es":{"name":"Síndrome autoinflamatorio piogénico de la infancia"},"it":{"name":"Sindrome autoinfiammatoria piogenica dell'infanzia"},"nl":{"name":"Pyogeen auto-inflammatoir syndroom van de kinderjaren"},"pt":{"name":"Síndrome autoinflamatória piogénica da infância"},"pl":{"name":"Dziecięcy zespół autozapalenia ropnego"},"cs":{"name":"Pyogenní autoinflamatorní syndrom v dětství"},"uk":{"name":"Піогенний аутозапальний синдром дитячого віку"},"zh":{"name":"儿童化脓性自体炎症综合征"},"tr":{"name":"Çocukluk çağı piyojenik otoinflamatuvar sendromu"}},"xrefs":[{"source":"MONDO","code":"0957404","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680953","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98023,"name":"Rare systemic or rheumatologic disease"},"parents":[{"orpha":319719,"name":"Autoinflammatory syndrome of childhood","classifications":[231]}],"children":[{"orpha":324964,"name":"Chronic nonbacterial osteomyelitis/Chronic recurrent multifocal osteomyelitis","type":"Disease"},{"orpha":404546,"name":"DITRA","type":"Disease"},{"orpha":251523,"name":"Hyperzincemia and hypercalprotectinemia","type":"Disease"},{"orpha":77297,"name":"Majeed syndrome","type":"Disease"},{"orpha":294023,"name":"Neonatal erythroderma-autoinflammation-inflammatory bowel disease syndrome","type":"Disease"},{"orpha":69126,"name":"PAPA syndrome","type":"Disease"},{"orpha":210115,"name":"Sterile multifocal osteomyelitis with periostitis and pustulosis","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}