raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:213500

Rare ovarian cancer

Synonyms: Rare ovarian malignant 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
LangNameSynonyms
enRare ovarian cancerRare ovarian malignant tumor
frCancer rare de l'ovaireTumeur maligne rare de l'ovaire
deSeltener EierstockkrebsOvarialkarzinom, seltenes · Seltener maligner Tumor der Eierstöcke
esCáncer de ovario raroTumor maligno de ovario raro
itTumore ovarico raroTumore ovarico maligno raro
nlZeldzame ovariumkankerZeldzame eierstokkanker · Zeldzame ovariële kwaadaardige tumor · Zeldzame ovariële maligne tumor
ptCancro do ovário raro
plRzadki rak jajnikaZłośliwy guz jajnika
csOvariální nádoryZhoubné nádory ovária
ukРак яєчниківЗлоякісна пухлина яєчників
zh卵巢癌卵巢恶性肿瘤
trYumurtalık kanseriOverin habis tümörü
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-112C73Especificvalidated
MONDO0008170Evalidated
MONDO8170Evalidated
MeSHD010051Evalidated
UMLSC1140680Evalidated
GARD7295Evalidated
MedDRA10033128Evalidated

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):

Children (2):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalence1-5 / 10 00049 / 100 000EuropeValue and classValidatedEuropean Medicines Agency 2018[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