raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:182114

Rare urogenital 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 urogenital tumor
frTumeur urogénitale rare
deUrogenitaler Tumor, seltener
esTumor urogenital raro
itTumore raro dell'apparato urogenitale
nlZeldzame urogenitale tumor
ptTumor urogenital raro
plRzadki guz układu moczowo-płciowego
csVzácné urogenitální nádory
ukРідкісна пухлина сечостатевої системи
zh罕见泌尿生殖肿瘤
trNadir ürogenital tümör
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO15931Evalidated
UMLSC5680591Evalidated

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 (3):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

2 records
TypeClassValueAreaQualificationValidationSource
Annual incidence1-9 / 1 000 0000.13 / 100 000EuropeValue and classNot yet validated22425262[PMID]
Annual incidence1-9 / 1 000 0000.21 / 100 000United StatesValue and classValidated22425262[PMID]

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