raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:101943

Rare hepatic and biliary tract 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 hepatic and biliary tract tumor
frTumeur rare du foie et des voies biliaires
deSeltener Gallengang- und Lebertumor
esTumor raro hepático y del tracto biliar
itTumore raro epatico e delle vie biliari
nlZeldzame tumor van lever en galwegen
ptTumor hepático, raro
plRzadkie guzy wątroby i dróg żółciowych
csVzácné nádory jater a žlučovodů
ukРідкісна пухлина печінки та жовчовивідних шляхів
zh罕见肝胆道肿瘤
trNadir karaciğer ve safra yolu tümörü
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO15117Evalidated
UMLSC5681783Evalidated
GARD19792Evalidated

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 (2):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card