{"orpha":181384,"name":"Rare 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-181384/","orphanet_url":"https://www.orpha.net/en/disease/detail/181384","names":{"fr":{"name":"Maladie hypophysaire ou hypothalamique rare"},"de":{"name":"Hypothalamus- oder Hypophysenkrankheit, seltene"},"es":{"name":"Enfermedad hipofisaria o hipotalámica rara"},"it":{"name":"Malattia rara dell'ipotalamo o dell'ipofisi"},"nl":{"name":"Zeldzame hypothalamische of hypofysaire ziekte"},"pt":{"name":"Doença hipotalâmica ou hipofisária rara","synonyms":["Doença hipotalâmica ou pituitária rara"]},"pl":{"name":"Rzadka choroba podwzgórza lub przysadki"},"cs":{"name":"Vzácné onemocnění hypotalamu nebo hypofýzy"},"uk":{"name":"Рідкісні захворювання гіпоталамуса або гіпофіза"},"zh":{"name":"罕见下丘脑或垂体疾病"},"tr":{"name":"Nadir hipotalamik veya hipofiz hastalığı"}},"xrefs":[{"source":"MONDO","code":"15889","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680477","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97978,"name":"Rare endocrine disease"},"parents":[{"orpha":97978,"name":"Rare endocrine disease","classifications":[193]}],"children":[{"orpha":689401,"name":"Acquired hypothalamic obesity","type":"Disease"},{"orpha":1672,"name":"Diencephalic syndrome","type":"Disease"},{"orpha":314621,"name":"Duplication of the pituitary gland","type":"Morphological anomaly"},{"orpha":715120,"name":"Hyperpituitarism","type":"Category"},{"orpha":443101,"name":"Hypothalamic adipsic hypernatraemia syndrome","type":"Disease"},{"orpha":101957,"name":"Pituitary deficiency","type":"Category"},{"orpha":525738,"name":"Prepubertal anorexia nervosa","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}