ORPHA:189424
OBSOLETE: ACTH-independent Cushing syndrome due to bilateral adrenocortical hyperplasia
inactive · referred to ORPHA:647758Adrenal Cushing syndrome
- Type
- Category
- 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 Adrenal Cushing syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: ACTH-independent Cushing syndrome due to bilateral adrenocortical hyperplasia | |
| fr | OBSOLETE : Syndrome de Cushing indépendant de l'ACTH du à une hyperplasie adrénocorticale bilatérale | |
| de | OBSOLET: Cushing-Syndrom, ACTH-unabhängiges, durch bilaterale Nebennierenrindenhyperplasie | |
| es | OBSOLETO: Síndrome de Cushing ACTH-independiente debido a hiperplasia adrenocortical | |
| it | OBSOLETO: Sindrome di Cushing ACTH-indipendente da iperplasia adrenocorticale bilaterale | |
| nl | OBSOLEET: ACTH-onafhankelijk syndroom van Cushing door bilaterale adrenocorticale hyperplasie | OBSOLEET: ACTH-onafhankelijk syndroom van Cushing door bilaterale bijnierschorshyperplasie |
| pt | OBSOLETO: Síndrome de Cushing independente da ACTH por hiperplasia adrenocortical bilateral | |
| pl | NIEAKTUALNE: Zespól Cushinga niezalezny od ACTH z powodu obustronnej hipoplazji kory nadnerczy | |
| cs | NEAKTUÁLNÍ: Cushingův syndrom nezávislý na ACTH způsobený bilaterální hyperplázií kůry nadledvinek | |
| uk | ЗАСТАРІЛО: АКТГ-незалежний синдром Кушинга внаслідок двобічної адренокортикальної гіперплазії | |
| zh | 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 | Eski adı: Bilateral adrenokortikal hiperplaziye bağlı ACTH-bağımsız Cushing sendromu |
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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/189424
- This record as JSON: /data/d/189424.json