{"orpha":183628,"name":"Rare genetic hypothalamic or pituitary 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-183628/","orphanet_url":"https://www.orpha.net/en/disease/detail/183628","names":{"fr":{"name":"Maladie hypophysaire ou hypothalamique rare d'origine génétique"},"de":{"name":"Hypothalamus- oder Hypophysenkrankheit, genetisch bedingte, seltene"},"es":{"name":"Enfermedad hipofisaria o hipotalámica rara de origen genético"},"it":{"name":"Malattia genetica rara dell'ipotalamo e dell'ipofisi"},"nl":{"name":"Zeldzame genetische hypothalamische of hypofysaire ziekte"},"pt":{"name":"Doença genética hipotalâmica ou pituitária rara"},"pl":{"name":"Rzadka genetyczna choroba przysadki lub podwzgórza"},"cs":{"name":"Vzácné dědičné onemocnění hypotalamu nebo hypofýzy"},"uk":{"name":"Рідкісні генетично обумовлені захворювання гіпоталамуса або гіпофіза"},"zh":{"name":"罕见遗传性下丘脑或垂体疾病"},"tr":{"name":"Nadir genetik hipotalamik veya hipofiz hastalığı"}},"xrefs":[{"source":"MONDO","code":"15968","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680536","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":397685,"name":"Familial hyperprolactinemia","type":"Disease"},{"orpha":181393,"name":"Growth hormone insensitivity syndrome","type":"Category"},{"orpha":101957,"name":"Pituitary deficiency","type":"Category"},{"orpha":300373,"name":"X-linked acrogigantism","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}