raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:217071

Renal cell carcinoma

Synonyms: RCC

Type
Clinical group
Group
Group of disorders
Inheritance
Not applicable
Age of onset
Adult
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
LangNameSynonyms
enRenal cell carcinomaRCC
frCarcinome rénal= en
deNierenzellkarzinom= en
esCarcinoma de células renalesCCR
itCarcinoma delle cellule renali= en
nlNiercelcarcinoomRCC · Renaalcelcarcinoom
ptCarcinoma de células renais
plRak nerkowokomórkowy= en
csKarcinom ledviny= en
ukНирково-клітинна карцинома= en
zh肾细胞癌= en
trRenal hücreli karsinomSSB
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-112C90.0Especificvalidated
MONDO0005086Evalidated
MONDO5086Evalidated
MeSHD002292Evalidated
UMLSC0007134Evalidated
GARD13215Evalidated
MedDRA10067946Evalidated

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 (2):

Children (9):

Codes that Orphanet moved or referred to this one:

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

2 records
TypeClassValueAreaQualificationValidationSource
Point prevalence1-5 / 10 00042 / 100 000EuropeValue and classValidatedEuropean Medicines Agency 2010[OTHER]
Annual incidence1-9 / 100 0008.35 / 100 000EuropeValue and classValidatedRARECARE surveillance of rare cancers in Europe[OTHER]

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.

7

Sources for this card