{"orpha":596426,"name":"Syndrome of reduced sensitivity to thyroid hormone","type":"Clinical group","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-596426/","orphanet_url":"https://www.orpha.net/en/disease/detail/596426","names":{"fr":{"name":"Syndrome de sensibilité réduite aux hormones thyroïdiennes"},"de":{"name":"Syndrome mit reduzierter Sensitivität gegenüber Schilddrüsenhormon"},"es":{"name":"Síndromes de sensibilidad reducida a las hormonas tiroideas"},"it":{"name":"Sindromi da ridotta sensibilità agli ormoni tiroidei","synonyms":["RTH"]},"nl":{"name":"Syndromen van gereduceerde gevoeligheid voor schildklierhormoon","synonyms":["RTH"]},"pt":{"name":"Síndromes de sensibilidade reduzida à hormona tiroideia","synonyms":["RTH"]},"pl":{"name":"Zespoły z obniżoną wrażliwością na hormony tarczycy"},"cs":{"name":"Syndrom snížené citlivosti na hormony štítné žlázy"},"uk":{"name":"Синдром зниженої чутливості до гормонів щитовидної залози"},"zh":{"name":"Syndrome of reduced sensitivity to thyroid hormone"},"tr":{"name":"Syndrome of reduced sensitivity to thyroid hormone"}},"xrefs":[{"source":"UMLS","code":"C4722330","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":59,"name":"Allan-Herndon-Dudley syndrome","type":"Disease"},{"orpha":597939,"name":"Euthyroid dysprealbuminemic hyperthyroxinemia","type":"Disease"},{"orpha":566231,"name":"Resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha","type":"Disease"},{"orpha":566243,"name":"Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta","type":"Disease"},{"orpha":171706,"name":"Short stature-delayed bone age due to thyroid hormone metabolism deficiency","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}