{"orpha":329888,"name":"Juvenile idiopathic inflammatory myopathy","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["JIIM"],"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-329888/","orphanet_url":"https://www.orpha.net/en/disease/detail/329888","names":{"fr":{"name":"Myopathie inflammatoire idiopathique juvénile","synonyms":["JIIM","MIIJ"]},"de":{"name":"Myopathie, idiopathische inflammatorische, juvenile Form","synonyms":["JIIM"]},"es":{"name":"Miopatía inflamatoria idiopática juvenil","synonyms":["JIIM"]},"it":{"name":"Miopatia infiammatoria idiopatica giovanile","synonyms":["JIIM"]},"nl":{"name":"Juveniele idiopathische inflammatoire myopathie","synonyms":["JIIM"]},"pt":{"name":"Miopatia inflamatória idiopática juvenil"},"pl":{"name":"Młodzieńcza idiopatyczna miopatia zapalna","synonyms":["JIIM"]},"cs":{"name":"Juvenilní idiopatická zánětlivá myopatie","synonyms":["JIIM"]},"uk":{"name":"Ювенільна ідіопатична запальна міопатія","synonyms":["JIIM"]},"zh":{"name":"青少年特发性炎性肌病","synonyms":["JIIM"]},"tr":{"name":"Juvenil idiyopatik inflamatuar miyopati","synonyms":["JIIM"]}},"xrefs":[{"source":"MONDO","code":"0018010","qualifier":"E","icd_relation":null,"validated":true},{"source":"MONDO","code":"18010","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5679857","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":98482,"name":"Idiopathic inflammatory myopathy","classifications":[181,196]}],"children":[{"orpha":93672,"name":"Juvenile dermatomyositis","type":"Disease"},{"orpha":329894,"name":"Juvenile overlap myositis","type":"Disease"},{"orpha":93568,"name":"Juvenile polymyositis","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}