raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:424933

Rare malignant epithelial tumor of liver and intrahepatic biliary tract

Synonyms: Rare malignant epithelial tumor of liver and IBT

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 malignant epithelial tumor of liver and intrahepatic biliary tractRare malignant epithelial tumor of liver and IBT
frTumeur épithéliale maligne rare du foie et des voies biliaires intrahépatiquesTumeur épithéliale maligne rare du foie et des VBIH
deSeltener maligner epithelialer Tumor der Leber und intrahepatischen Gallengänge
esTumor epitelial maligno raro de hígado y vías biliares intrahepáticasTumor epitelial maligno raro de hígado y VBI
itTumore epiteliale raro del fegato e delle vie biliari intraepaticheTumore epiteliale del fegato e delle VBI
nlZeldzame maligne epitheliale tumor van lever en intrahepatische galwegenZeldzame maligne epitheliale tumor van lever en IBT
ptTumor epitelial maligno raro do fígado e trato biliar intra-hepático
plRzadki nabłonkowy guz wątroby i wewnątrzwątrobowego przewodu żółciowegoRzadki nabłonkowy guz wątroby i IBT
csVzácné epiteliální tumory jater a intrahepatálních žlučových cestVzácný epiteliální nádor jater a IBT
ukРідкісна злоякісна епітеліальна пухлина печінки та внутрішньопечінкових жовчних шляхівРідкісна злоякісна епітеліальна пухлина печінки та IBT
zh肝和肝内胆道罕见恶性上皮肿瘤罕见恶性上皮肝癌和IBT
trKaraciğer ve intrahepatik safra yollarının nadir habis epitel tümörüNadir habis epitel tümörü ve IBT
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO18530Evalidated
UMLSC5680080Evalidated

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

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