{"orpha":280373,"name":"Rare pediatric systemic 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-280373/","orphanet_url":"https://www.orpha.net/en/disease/detail/280373","names":{"fr":{"name":"Maladie systémique rare de l'enfant"},"de":{"name":"Seltene systemische Krankheit des Kindes"},"es":{"name":"Enfermedad sistémica pediátrica rara"},"it":{"name":"Malattia sistemica pediatrica"},"nl":{"name":"Zeldzame pediatrische systemische ziekte"},"pt":{"name":"Doença sistémica pediátrica rara"},"pl":{"name":"Rzadka dziecięca choroba układowa"},"cs":{"name":"Systémová onemocnění v pediatrii"},"uk":{"name":"Рідкісне дитяче системне захворювання"},"zh":{"name":"罕见小儿系统性疾病"},"tr":{"name":"Nadir pediatrik sistemik hastalık"}},"xrefs":[{"source":"UMLS","code":"C5680784","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98023,"name":"Rare systemic or rheumatologic disease"},"parents":[{"orpha":280342,"name":"Rare systemic or rheumatological disease of childhood","classifications":[231]}],"children":[{"orpha":444463,"name":"Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency","type":"Disease"},{"orpha":444092,"name":"Autoimmune interstitial lung disease-arthritis syndrome","type":"Disease"},{"orpha":3165,"name":"Eosinophilic fasciitis","type":"Disease"},{"orpha":337,"name":"Fibrodysplasia ossificans progressiva","type":"Disease"},{"orpha":93672,"name":"Juvenile dermatomyositis","type":"Disease"},{"orpha":93568,"name":"Juvenile polymyositis","type":"Disease"},{"orpha":598363,"name":"Multisystem inflammatory syndrome in children and adults","type":"Disease"},{"orpha":251312,"name":"Overlapping connective tissue disease","type":"Clinical group"},{"orpha":300359,"name":"PLCG2-associated antibody deficiency and immune dysregulation","type":"Disease"},{"orpha":93552,"name":"Pediatric systemic lupus erythematosus","type":"Disease"},{"orpha":438159,"name":"STAT3-related early-onset multisystem autoimmune disease","type":"Disease"},{"orpha":797,"name":"Sarcoidosis","type":"Disease"},{"orpha":398091,"name":"Secondary neonatal autoimmune disease","type":"Category"},{"orpha":90291,"name":"Systemic sclerosis","type":"Disease"},{"orpha":251332,"name":"Unexplained long-lasting fever/inflammatory syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}