{"orpha":181399,"name":"Rare hyperthyroidism","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-181399/","orphanet_url":"https://www.orpha.net/en/disease/detail/181399","names":{"fr":{"name":"Hyperthyroïdie rare"},"de":{"name":"Hyperthyreose, seltene"},"es":{"name":"Hipertiroidismo raro"},"it":{"name":"Ipertiroidismo raro"},"nl":{"name":"Zeldzame hyperthyreoïdie"},"pt":{"name":"Hipertiroidismo raro"},"pl":{"name":"Rzadka postać nadczynności tarczycy"},"cs":{"name":"Vzácný hypertyreoidismus"},"uk":{"name":"Рідкісний гіпертиреоз"},"zh":{"name":"罕见甲状腺功能亢进症"},"tr":{"name":"Nadir hipertiroidi"}},"xrefs":[{"source":"MONDO","code":"15894","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680610","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":183631,"name":"Rare genetic thyroid disease","classifications":[156]},{"orpha":101955,"name":"Rare thyroid disease","classifications":[193]}],"children":[{"orpha":99819,"name":"Familial gestational hyperthyroidism","type":"Disease"},{"orpha":424,"name":"Familial hyperthyroidism due to mutations in TSH receptor","type":"Disease"},{"orpha":525731,"name":"Pediatric-onset Graves disease","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}