ORPHA:631251
Cancer of unknown primary site
Synonyms: CUP · Carcinoma of unknown primary · Carcinoma of unknown primary origin · Metastases without primary tumor
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cancer of unknown primary site | CUP · Carcinoma of unknown primary · Carcinoma of unknown primary origin · Metastases without primary tumor |
| fr | Cancer de primitif inconnu | Cancer primitif inconnu |
| de | Krebserkrankung mit unbekanntem Primärtumor | CUP · CUP-Syndrom · Karzinom unbekannter primärer Herkunft · Metastasen bei unbekanntem Primärtumor |
| es | Cáncer de origen primario desconocido | Carcinoma de origen primario desconocido · Metástasis sin tumor primario |
| it | Neoplasia con sede primaria ignota | CUP · Carcinoma ad origine primitiva ignota · Carcinoma con sede primitiva ignota · Metastasi senza tumore primitivo |
| nl | Kanker van onbekende oorsprong | CUP · Carcinoom van onbekende oorsprong · Metastasen zonder primaire tumor |
| pt | Cancro de localização primária desconhecida | CUP · Carcinoma de origem primária desconhecida · Metástases sem tumor primário |
| pl | Nowotwór o nieznanym punkcie wyjścia | Nowotwór o nieznanym ognisku pierwotnym |
| cs | Nádorové onemocnění neznámé primární lokalizace | = en |
| uk | Рак невідомої первинної локалізації | Карцинома невідомої первинної локалізації · Карцинома невідомого первинного походження · CUP · Метастази без первинної пухлини |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C80.0 | NTBT | attributed | validated |
| ICD-11 | 2D44 | NTBT | attributed | validated |
| MONDO | 0858997 | E | validated | |
| UMLS | C0220647 | 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:98057Rare tumor
rare neoplastic diseases
No children.
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/631251
- This record as JSON: /data/d/631251.json