ORPHA:306633

Rare tumor of gallbladder and extrahepatic biliary tract

Synonyms: Rare tumor of gallbladder and EBT

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.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Rare tumor of gallbladder and extrahepatic biliary tract	Rare tumor of gallbladder and EBT
fr	Tumeur rare de la vésicule biliaire et des voies biliaires extrahépatiques	Tumeur rare de la vésicule biliaire et des VBEH
de	Seltener Tumor der Gallenblase und extrahepatischen Gallengänge
es	Tumor raro de vesícula y vías biliares extrahepáticas	Tumor raro de vesícula y VBE
it	Tumore raro della cistifellea e delle vie biliari extraepatiche	Tumore raro della cistifellea e delle VBE
nl	Zeldzame tumor van de galblaas en extrahepatische galwegen	Zeldzame tumor van de galblaas en EBT
pt	Tumor raro de vias biliares
pl	Rzadki guz pęcherzyka żółciowego i zewnątrzwątrobowych przewodów żółciowych	Rzadki guz pęcherzyka żółciowego i EBT
cs	Vzácné nádory žlučníku a extrahepatálních žlučových cest	Vzácné nádory žlučníku a EBT
uk	Рідкісна пухлина жовчного міхура та позапечінкових жовчовивідних шляхів	Рідкісна пухлина жовчного міхура та EBT
zh	胆囊及肝外胆道罕见肿瘤	胆囊及肝外胆道罕见肿瘤
tr	Nadir safra kesesi ve ekstrahepatik safra yolu tümörü	Nadir safra kesesi tümörü ve EBT

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	17631	E		validated
UMLS	C5679980	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Classification

Preferential parent (Orphanet linearisation):

ORPHA:250908Rare neoplastic disease

Parents in the classifications (1):

ORPHA:101943Rare hepatic and biliary tract tumor
rare hepatic diseases; rare neoplastic diseases

Children (2):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

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

Sources for this card

Orphanet page: orpha.net/en/disease/detail/306633
This record as JSON: /data/d/306633.json