{"orpha":553,"name":"OBSOLETE: Cushing syndrome","type":"Clinical group","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Hyperadrenocorticism","OBSOLETE: Hypercortisolism"],"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 Endogenous Cushing syndrome","url":"https://raremap.alftech.space/d/ORPHA-553/","orphanet_url":"https://www.orpha.net/en/disease/detail/553","names":{"fr":{"name":"OBSOLETE : Syndrome de Cushing","synonyms":["OBSOLETE : Hyperadrénocorticisme","OBSOLETE : Hypercortisolisme"]},"de":{"name":"OBSOLET: Cushing-Syndrom","synonyms":["OBSOLET: Hyperadrenokortizismus","OBSOLET: Hyperkortisolismus"]},"es":{"name":"OBSOLETO: Síndrome de Cushing","synonyms":["OBSOLETO: Hiperadrenocorticismo","OBSOLETO: Hipercortisolismo"]},"it":{"name":"OBSOLETO: Sindrome di Cushing","synonyms":["OBSOLETO: Iperadrenocorticismo","OBSOLETO: Ipercortisolismo"]},"nl":{"name":"OBSOLEET: Syndroom van Cushing","synonyms":["OBSOLEET: Hyperadrenocorticisme","OBSOLEET: Hypercortisolisme"]},"pt":{"name":"OBSOLETO: Síndrome Cushing","synonyms":["OBSOLETO: Hiperadrenocorticismo","OBSOLETO: Hipercortisolismo"]},"pl":{"name":"NIEAKTUALNE: Zespół Cushinga","synonyms":["NIEAKTUALNE: Hiperadrenokortycyzm","NIEAKTUALNE: Hiperkortyzolizm","NIEAKTUALNE: Zespół Cushinga"]},"cs":{"name":"NEAKTUÁLNÍ: Cushingův syndrom","synonyms":["NEAKTUÁLNÍ: Hyperadrenokorticismus","NEAKTUÁLNÍ: Hyperkortizolismus"]},"uk":{"name":"ЗАСТАРІЛО: Синдром Кушинга","synonyms":["ЗАСТАРІЛО: Гіперадренокортицизм","ЗАСТАРІЛО: Гіперкортицизм"]},"zh":{"name":"库欣综合征","synonyms":["肾上腺皮质功能亢进"]},"tr":{"name":"Cushing sendromu","synonyms":["Hiperkortizolizm","Hiperadrenokortizm"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":641613,"name":"Endogenous Cushing syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}