ORPHA:100091
Adrenal/paraganglial tumor
- Type
- Category
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Adrenal/paraganglial tumor | |
| fr | Tumeur des surrénales/paraganglions | |
| de | Tumor, adrenaler/paraganglialer | |
| es | Tumor suprarrenal/paraganglial | |
| it | Tumore surrenale/paragangliare | |
| nl | Adrenale/paragangliale tumor | |
| pt | Tumor supra-renal/paraganglial | |
| pl | Guz nadnerczy/nerwiak przyzwojowy | |
| cs | Adrenální/paragangliální nádor | |
| uk | Пухлина наднирників/парагангліїв | |
| zh | 肾上腺/神经节旁肿瘤 | |
| tr | Adrenal / paraganglial tümör |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681806 | E | validated | |
| GARD | 19765 | 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 (2):
- ORPHA:101954Rare adrenal disease
rare endocrine diseases - ORPHA:182130Tumor of endocrine glands
rare neoplastic diseases
Children (10):
- ORPHA:1501Adrenocortical carcinoma
- ORPHA:1359Carney complex
- ORPHA:404Familial hyperaldosteronism type II
- ORPHA:652Multiple endocrine neoplasia type 1
- ORPHA:247698Multiple endocrine neoplasia type 2A
- ORPHA:247709Multiple endocrine neoplasia type 2B
- ORPHA:573163Pheochromocytoma-paraganglioma
- ORPHA:91351Pituitary dermoid and epidermoid cysts
- ORPHA:649017Rare adrenocortical nodular disease
- ORPHA:892Von Hippel-Lindau disease
Codes that Orphanet moved or referred to this one:
- ORPHA:717OBSOLETE: Catecholamine-producing tumor referred to · inactive
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/100091
- This record as JSON: /data/d/100091.json