ORPHA:443287
OBSOLETE: ACTH-independent Cushing syndrome due to rare cortisol-producing adrenal tumor
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 rare cortisol-producing adrenal tumor | |
| fr | OBSOLETE : Syndrome de Cushing indépendant de l'ACTH dû à une tumeur rare surrénalienne sécrétrice de cortisol | |
| de | OBSOLET: Cushing-Syndrom, ACTH-unabhängiges, durch Cortisol-produzierenden Nebennierentumor | |
| es | OBSOLETO: Síndrome de Cushing independiente de ACTH por tumor suprarrenal raro productor de cortisol | |
| it | OBSOLETO: Sindrome di Cushing ACTH-independente da tumore surrenale raro producente cortisolo | |
| nl | OBSOLEET: ACTH-onafhankelijk syndroom van Cushing door zeldzame cortisolproducerende adrenale tumor | |
| pt | OBSOLETO: Síndrome Cushing ACTH-independente por tumor supra-renal produtor de cortisol raro | |
| pl | NIEAKTUALNE: Zespół Cushinga niezależny od ACTH związany z rzadkim guzem nadnercza produkującym kortyzol | |
| cs | NEAKTUÁLNÍ: ACTH-independentní Cushingův syndrom způsobený vzácným kortizol produkujícím nádorem | |
| uk | ЗАСТАРІЛО: АКТГ-незалежний синдром Кушинга, зумовлений рідкісною пухлиною надниркових залоз, що продукує кортизол | |
| zh | 罕见产皮质醇肾上腺肿瘤所致ACTH非依赖性库欣综合征 | |
| tr | Nadir kortizol üreten adrenal tümöre 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/443287
- This record as JSON: /data/d/443287.json