ORPHA:649017
Rare adrenocortical nodular disease
- 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 | |
| fr | Maladie nodulaire corticosurrénalienne rare | Maladie nodulaire cortico-surrénalienne rare |
| de | Seltene adrenokortikale noduläre Krankheit | Seltene noduläre Nebennierenrindenerkrankung |
| es | Enfermedad corticosuprarrenal nodular rara | |
| it | Malattia rara nodulare adrenocorticale | |
| nl | Zeldzame adrenocorticale nodulaire ziekte | |
| pt | Doença adrenocortical nodular rara | |
| pl | Rzadka choroba guzkowa kory nadnerczy | |
| cs | Vzácné adrenokortikální nodulární onemocnění | |
| uk | Рідкісна хвороба кори надниркових залоз |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5816740 | 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:100091Adrenal/paraganglial tumor
rare endocrine diseases; rare neoplastic 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/649017
- This record as JSON: /data/d/649017.json