raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
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
LangNameSynonyms
enCancer of unknown primary siteCUP · Carcinoma of unknown primary · Carcinoma of unknown primary origin · Metastases without primary tumor
frCancer de primitif inconnuCancer primitif inconnu
deKrebserkrankung mit unbekanntem PrimärtumorCUP · CUP-Syndrom · Karzinom unbekannter primärer Herkunft · Metastasen bei unbekanntem Primärtumor
esCáncer de origen primario desconocidoCarcinoma de origen primario desconocido · Metástasis sin tumor primario
itNeoplasia con sede primaria ignotaCUP · Carcinoma ad origine primitiva ignota · Carcinoma con sede primitiva ignota · Metastasi senza tumore primitivo
nlKanker van onbekende oorsprongCUP · Carcinoom van onbekende oorsprong · Metastasen zonder primaire tumor
ptCancro de localização primária desconhecidaCUP · Carcinoma de origem primária desconhecida · Metástases sem tumor primário
plNowotwór o nieznanym punkcie wyjściaNowotwór o nieznanym ognisku pierwotnym
csNádorové onemocnění neznámé primární lokalizace= en
ukРак невідомої первинної локалізаціїКарцинома невідомої первинної локалізації · Карцинома невідомого первинного походження · CUP · Метастази без первинної пухлини
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C80.0NTBTattributedvalidated
ICD-112D44NTBTattributedvalidated
MONDO0858997Evalidated
UMLSC0220647Evalidated

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):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card