raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:363579

Extragonadal germ cell 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
enExtragonadal germ cell tumor
frTumeur germinale extragonadique
deKeimzelltumor, extragonadaler
esTumores extragonadales de células germinales
itTumore extragonadico delle cellule germinali
nlExtragonadale kiemceltumor
ptTumor de células germinativas extragonadal
plGuz zarodkowy pozagonadalny
csExtragonadální germinální nádor
ukЕкстрагонадна герміногенна пухлина
zh性腺外生殖细胞瘤
trEkstragonadal germ hücreli tümör
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO0018201Evalidated
MONDO18201Evalidated
UMLSC0262963Evalidated
GARD9325Evalidated

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 (3):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Annual incidence1-9 / 1 000 0000.13 / 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