ORPHA:553
OBSOLETE: Cushing syndrome
inactive · referred to ORPHA:641613Endogenous Cushing syndrome
Synonyms: OBSOLETE: Hyperadrenocorticism · OBSOLETE: Hypercortisolism
- Type
- Clinical group
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
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
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Cushing syndrome | OBSOLETE: Hyperadrenocorticism · OBSOLETE: Hypercortisolism |
| fr | OBSOLETE : Syndrome de Cushing | OBSOLETE : Hyperadrénocorticisme · OBSOLETE : Hypercortisolisme |
| de | OBSOLET: Cushing-Syndrom | OBSOLET: Hyperadrenokortizismus · OBSOLET: Hyperkortisolismus |
| es | OBSOLETO: Síndrome de Cushing | OBSOLETO: Hiperadrenocorticismo · OBSOLETO: Hipercortisolismo |
| it | OBSOLETO: Sindrome di Cushing | OBSOLETO: Iperadrenocorticismo · OBSOLETO: Ipercortisolismo |
| nl | OBSOLEET: Syndroom van Cushing | OBSOLEET: Hyperadrenocorticisme · OBSOLEET: Hypercortisolisme |
| pt | OBSOLETO: Síndrome Cushing | OBSOLETO: Hiperadrenocorticismo · OBSOLETO: Hipercortisolismo |
| pl | NIEAKTUALNE: Zespół Cushinga | NIEAKTUALNE: Hiperadrenokortycyzm · NIEAKTUALNE: Hiperkortyzolizm · NIEAKTUALNE: Zespół Cushinga |
| cs | NEAKTUÁLNÍ: Cushingův syndrom | NEAKTUÁLNÍ: Hyperadrenokorticismus · NEAKTUÁLNÍ: Hyperkortizolismus |
| uk | ЗАСТАРІЛО: Синдром Кушинга | ЗАСТАРІЛО: Гіперадренокортицизм · ЗАСТАРІЛО: Гіперкортицизм |
| zh | 库欣综合征 | 肾上腺皮质功能亢进 |
| tr | Cushing sendromu | Hiperkortizolizm · Hiperadrenokortizm |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/553
- This record as JSON: /data/d/553.json