raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:647758

Adrenal Cushing syndrome

Synonyms: Adrenal CS

Type
Clinical group
Group
Group of disorders
Status
active

A group of endogenous Cushing syndrome (CS) that may result from excess secretion of cortisol by either a unilateral and benign (adrenocortical adenoma), or malignant (adrenocortical carcinoma) adrenocortical tumor, or nodular adrenocortical disease, including Cushing syndrome due to bilateral macronodular adrenocortical disease (BMAD), isolated micronodular adrenocortical disease (i-MAD) and primary pigmented nodular adrenocortical disease (PPNAD; isolated or in Carney complex).

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Names in Orphadata languages

10 of 12 languages
LangNameSynonyms
enAdrenal Cushing syndromeAdrenal CS
frSyndrome de Cushing surrénalien
deAdrenales Cushing-SyndromAdrenales CS
esSíndrome de Cushing suprarrenalSC suprarrenal
itSindrome di Cushing surrenalicaSC surrenalica
nlAdrenaal syndroom van CushingAdrenaal CS · Syndroom van Cushing met oorzaak in bijnier
ptSíndrome Cushing supra-renalCS supra-renal
plZespół Cushinga pochodzenia nadnerczowego= en
csAdrenální Cushingův syndrom= en
ukАдренальний синдром Кушинга= en

Definition in:

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Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
UMLSC0342443Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

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Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (3):

Codes that Orphanet moved or referred to this one:

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Genes

0 direct

Orphanet records no gene directly on this code.

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Prevalence and incidence

0 records

No 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