ORPHA:573163
Pheochromocytoma-paraganglioma
- Type
- Clinical group
- Group
- Group of disorders
- Status
- active
A rare neuroendocrine tumor arising from chromaffin cells of the adrenal medulla (pheochromocytoma) or from sympathetic and parasympathetic ganglia (paraganglioma). These tumors are most often benign and may produce catecholamines in excess causing hypertension and sometimes severe acute cardiovascular complications.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Pheochromocytoma-paraganglioma | |
| fr | Phéochromocytome-paragangliome | |
| de | Phaeochromozytom-Paragangliom-Syndrom | |
| es | Feocromocitoma-paraganglioma | |
| it | Feocromocitoma-paraganglioma | |
| nl | Feochromocytoom-paraganglioom | |
| pt | Feocromocitoma-paraganglioma | |
| pl | Guz chromochłonny nadnercza i przyzwojak | |
| cs | Feochromocytom-paragangliom | |
| uk | Феохромоцитома-парагангліома | |
| zh | 嗜铬细胞瘤-副神经节瘤 | |
| tr | Feokromositom-paragangliom |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0035540 | E | validated | |
| UMLS | C5681712 | E | validated |
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):
- ORPHA:100091Adrenal/paraganglial tumor
rare endocrine diseases; rare neoplastic diseases
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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/573163
- This record as JSON: /data/d/573163.json