{"orpha":189424,"name":"OBSOLETE: ACTH-independent Cushing syndrome due to bilateral adrenocortical hyperplasia","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Adrenal Cushing syndrome","url":"https://raremap.alftech.space/d/ORPHA-189424/","orphanet_url":"https://www.orpha.net/en/disease/detail/189424","names":{"fr":{"name":"OBSOLETE : Syndrome de Cushing indépendant de l'ACTH du à une hyperplasie adrénocorticale bilatérale"},"de":{"name":"OBSOLET: Cushing-Syndrom, ACTH-unabhängiges, durch bilaterale Nebennierenrindenhyperplasie"},"es":{"name":"OBSOLETO: Síndrome de Cushing ACTH-independiente debido a hiperplasia adrenocortical"},"it":{"name":"OBSOLETO: Sindrome di Cushing ACTH-indipendente da iperplasia adrenocorticale bilaterale"},"nl":{"name":"OBSOLEET: ACTH-onafhankelijk syndroom van Cushing door bilaterale adrenocorticale hyperplasie","synonyms":["OBSOLEET: ACTH-onafhankelijk syndroom van Cushing door bilaterale bijnierschorshyperplasie"]},"pt":{"name":"OBSOLETO: Síndrome de Cushing independente da ACTH por hiperplasia adrenocortical bilateral"},"pl":{"name":"NIEAKTUALNE: Zespól Cushinga niezalezny od ACTH z powodu obustronnej hipoplazji kory nadnerczy"},"cs":{"name":"NEAKTUÁLNÍ: Cushingův syndrom nezávislý na ACTH způsobený bilaterální hyperplázií kůry nadledvinek"},"uk":{"name":"ЗАСТАРІЛО: АКТГ-незалежний синдром Кушинга внаслідок двобічної адренокортикальної гіперплазії"},"zh":{"name":"弃用：双侧肾上腺皮质增生所致非肾上腺皮质激素依赖的库欣综合征"},"tr":{"name":"Eski adı: Bilateral adrenokortikal hiperplaziye bağlı ACTH-bağımsız Cushing sendromu"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":647758,"name":"Adrenal Cushing syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}