raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:180226

Embryonal carcinoma

Type
Disease
Group
Disorder
Inheritance
Not applicable
Age of onset
Adolescent, Childhood
Status
active

Orphadata ships no English definition for this code.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enEmbryonal carcinoma
frCarcinome embryonnaire
deEmbryonales Karzinom
esCarcinoma embrionario
itCarcinoma embrionale
nlEmbryonaal carcinoom
ptCarcinoma embrionário
plRak embrionalny
csEmbryonální karcinom
ukЕмбріональна карцинома
zh胚胎癌
trEmbriyonal karsinom
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C22.7BTNTattributedvalidated
ICD-10C71.9BTNTattributedvalidated
MONDO0005440Evalidated
MeSHD018236Evalidated
UMLSC0206659Evalidated
GARD5140Evalidated

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
Annual incidence<1 / 1 000 0000.01 / 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