{"orpha":183631,"name":"Rare genetic 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-183631/","orphanet_url":"https://www.orpha.net/en/disease/detail/183631","names":{"fr":{"name":"Maladie rare de la thyroïde d'origine génétique"},"de":{"name":"Schilddrüsenkrankheit, genetisch bedingte, seltene"},"es":{"name":"Enfermedad rara de la tiroides de origen genético"},"it":{"name":"Malattia genetica rara della tiroide"},"nl":{"name":"Zeldzame genetische schildklierziekte"},"pt":{"name":"Doença da tiroide genética rara"},"pl":{"name":"Rzadka genetyczna choroba tarczycy"},"cs":{"name":"Vzácná geneticky podmíněná onemocnění štítné žlázy"},"uk":{"name":"Рідкісне генетично обумовлене захворювання щитовидної залози"},"zh":{"name":"罕见遗传性甲状腺疾病"},"tr":{"name":"Nadir genetik tiroid hastalığı"}},"xrefs":[{"source":"MONDO","code":"15969","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680539","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":156638,"name":"Rare genetic endocrine disease","classifications":[156]}],"children":[{"orpha":276399,"name":"Familial multinodular goiter","type":"Disease"},{"orpha":181399,"name":"Rare hyperthyroidism","type":"Category"},{"orpha":181396,"name":"Rare hypothyroidism","type":"Category"},{"orpha":596426,"name":"Syndrome of reduced sensitivity to thyroid hormone","type":"Clinical group"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}