ORPHA:647768
Rare adrenocortical nodular disease with Cushing syndrome as a major feature
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
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.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare adrenocortical nodular disease with Cushing syndrome as a major feature | |
| fr | Maladie nodulaire corticosurrénalienne rare avec un syndrome de Cushing comme manifestation majeure | Maladie nodulaire cortico-surrénalienne rare avec un syndrome de Cushing comme manifestation majeure |
| de | Seltene noduläre Nebennierenrindenerkrankungen mit Cushing-Syndrom als Hauptmerkmal | |
| es | Enfermedad nodular corticosuprarrenal rara con síndrome de Cushing como característica principal | Enfermedad nodular adrenocortical rara con síndrome de Cushing como característica principal |
| it | Malattia rara adrenocorticale nodulare con sindrome di Cushing come caratteristica principale | |
| nl | Zeldzame adrenocorticale nodulaire ziekte met syndroom van Cushing als hoofdkenmerk | |
| pt | Doença adrenocortical nodular rara com síndrome Cushing como característica principal | |
| pl | Rzadka choroba guzkowa kory nadnerczy z zespołem Cushinga jako główną cechą | |
| cs | Vzácné adrenokortikální nodulární onemocnění s Cushingovým syndromem jako hlavním příznakem | |
| uk | Рідкісне вузлове адренокортикальне захворювання з синдромом Кушинга як основною ознакою |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5816751 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:314749Rare disease with adrenal Cushing syndrome as a major feature
rare endocrine diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/647768
- This record as JSON: /data/d/647768.json