raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:424991

Adenocarcinoma of the gallbladder and extrahepatic biliary tract

Synonyms: Adenocarcinoma of the gallbladder and EBT

Type
Disease
Group
Disorder
Inheritance
Not applicable
Age of onset
Adult
Status
active

A rare epithelial carcinoma, arising either in the gallbladder itself or from the epithelium lining the extrahepatic biliary tree, cystic duct and/or peribiliary gland, characterized by nonspecific symptoms, such as abdominal pain, jaundice and vomiting and sometimes mimicking benign biliary diseases. Chronic biliary epithelial inflammation (e.g. primary sclerosing cholangitis, cholelithiasis, choledocholithiasis, liver fluke infestation) is a major risk factor.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enAdenocarcinoma of the gallbladder and extrahepatic biliary tractAdenocarcinoma of the gallbladder and EBT
frAdénocarcinome de la vésicule biliaire et des voies biliaires extrahépatiquesAdénocarcinome de la vésicule biliaire et des VBEH
deAdenokarzinom der Gallenblase und extrahepatischen GallengängeAdenokarzinom der Gallenblase und EBT
esAdenocarcinoma de la vesícula biliar y de las vías biliares extrahepáticasAdenocarcinoma de vesícula y VBE
itAdenocarcinoma della cistifellea e delle vie biliari extraepaticheAdenocarcinoma della cistifellea e delle VBE
nlAdenocarcinoom van galblaas en extrahepatische galwegenAdenocarcinoom van galblaas en EBT
ptAdenocarcinoma da vesícula biliar e do trato biliar extra-hepáticoAdenocarcinoma da vesícula biliar e do TBEH
plGruczolakorak pęcherzyka żółciowego i zewnątrzwątrobowego przewodu żółciowegoGruczolakorak pęcherzyka żółciowego i EBT
csAdenokarcinom žlučníku a extrahepatálních žlučových cestAdenokarcinom žlučníku a EBT
ukАденокарцинома жовчного міхура та позапечінкових жовчовивідних шляхівАденокарцинома жовчного міхура та EBT
zh胆囊和肝外胆道腺癌胆囊腺癌和EBT
trSafra kesesi adenokarsinomu ve ekstrahepatik safra yollarıSafra kesesi adenokarsinomu ve EBT

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10C23BTNTattributedvalidated
ICD-10C24.0BTNTattributedvalidated
ICD-10C24.1BTNTattributedvalidated
ICD-10C24.8BTNTattributedvalidated
MONDO0018536Evalidated
UMLSC4707555Evalidated

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):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Annual incidence1-9 / 100 0002.62 / 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