{"orpha":101955,"name":"Rare thyroid 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-101955/","orphanet_url":"https://www.orpha.net/en/disease/detail/101955","names":{"fr":{"name":"Maladie rare de la thyroïde"},"de":{"name":"Schilddrüsenkrankheit, seltene"},"es":{"name":"Enfermedad rara de la tiroides"},"it":{"name":"Malattia tiroidea rara"},"nl":{"name":"Zeldzame schildklierziekte"},"pt":{"name":"Doença da tiroide rara"},"pl":{"name":"Rzadkie choroby tarczycy"},"cs":{"name":"Vzácné tyreoidální onemocnění"},"uk":{"name":"Рідкісні захворювання щитовидної залози"},"zh":{"name":"罕见甲状腺疾病"},"tr":{"name":"Nadir tiroid hastalığı"}},"xrefs":[{"source":"MONDO","code":"15125","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681800","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19799","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":872,"name":"OBSOLETE: Disorder in the hormonal synthesis with or without goiter","status":"inactive"}],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":97978,"name":"Rare endocrine disease","classifications":[193]}],"children":[{"orpha":95718,"name":"Congenital thyroid malformation without hypothyroidism","type":"Category"},{"orpha":276399,"name":"Familial multinodular goiter","type":"Disease"},{"orpha":181399,"name":"Rare hyperthyroidism","type":"Category"},{"orpha":181396,"name":"Rare hypothyroidism","type":"Category"},{"orpha":100087,"name":"Rare thyroid tumor","type":"Category"},{"orpha":596426,"name":"Syndrome of reduced sensitivity to thyroid hormone","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}