ORPHA:100076
Duodenal neuroendocrine 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Duodenal neuroendocrine tumor | |
| fr | Tumeur neuroendocrine du duodénum | |
| de | Tumor, neuroendokriner, des Duodenums | |
| es | Tumor neuroendocrino del duodeno | |
| it | Tumore endocrino duodenale | |
| nl | Neuro-endocriene tumor van duodenum | Duodenale neuro-endocriene tumor · Neuro-endocriene tumor van twaalfvingerige darm |
| pt | Tumor endócrino do duodeno | |
| pl | Guz neuroendokrynny dwunastnicy | |
| cs | Duodenální endokrinní nádor | |
| uk | Нейроендокринна пухлина дванадцятипалої кишки | |
| zh | 十二指肠神经内分泌肿瘤 | |
| tr | Duodenal nöroendokrin tümör |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15063 | E | validated | |
| UMLS | C4525619 | 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:423975Neuroendocrine tumor of the small intestine
rare gastroenterological diseases; rare endocrine diseases; rare neoplastic diseases; rare transplant-related disorders
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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/100076
- This record as JSON: /data/d/100076.json