ORPHA:263339
Poorly differentiated thymic neuroendocrine carcinoma
- Type
- Histopathological subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
This disease is described under Thymic neuroendocrine carcinoma
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Poorly differentiated thymic neuroendocrine carcinoma | |
| fr | Carcinome neuroendocrine thymique peu différencié | CNET peu différencié |
| de | Thymuskarzinom, neuroendokrines, undifferenziert | |
| es | Carcinoma neuroendocrino tímico pobremente diferenciado | |
| it | Carcinoma neuroendocrino timico scarsamente differenziato | |
| nl | Slecht gedifferentieerd neuro-endocrien thymuscarcinoom | |
| pt | Carcinoma tímico neuroendócrino com reduzida diferenciação | |
| pl | Słabo zróżnicowany rak neuroendokrynny grasicy | |
| cs | Málo diferencovaný neuroendokrinní karcinom thymu | |
| uk | Погано диференційована нейроендокринна карцинома тимуса | |
| zh | 低分化胸腺神经内分泌癌 | |
| tr | Kötü diferansiye timik nöroendokrin karsinom |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C37 | NTBT | attributed | validated |
| ICD-11 | 2C27.1 | NTBT | index | validated |
| MONDO | 0016978 | E | validated | |
| UMLS | C4305466 | 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:99869Thymic neuroendocrine carcinoma
rare endocrine diseases; rare neoplastic diseases
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/263339
- This record as JSON: /data/d/263339.json