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Herb Integrative Database
Traditional Medicine Data Platform
Diseases

Intrahepatic Cholangiocarcinoma

intrahepatic cholangiocarcinoma

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Entity Type
Diseases
Relation Groups
3
Relation Preview
24

Basic Information

Grouped by core information, identifiers, and descriptions.

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Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Core Information

Disease Name
Intrahepatic Cholangiocarcinoma
Standard Disease Name
intrahepatic cholangiocarcinoma
MeSH Tree
No data
ICD-10
C22.1

Identifiers

DO ID
No data
MeSH ID
D018281
OMIM ID
No data
UMLS ID
C0345905
HPO ID
No data

Description and Extensions

Description
NCI2016_CDISC_1602D:A malignant neoplasm of the liver arising from/comprising cells resembling those of bile ducts.|NCI2016_02D:A carcinoma that arises from the intrahepatic bile duct epithelium in any site of the intrahepatic biliary tree. Grossly, the malignant lesions are solid, nodular, and grayish. Morphologically, the vast majority of cases are adenocarcinomas. Signs and symptoms include malaise, weight loss, right upper quadrant abdominal pain, and night sweats. Early detection is difficult and the prognosis is generally poor.|MSH2017_2016_08_12:A carcinoma that originates in the intrahepatic bile duct epithelium of the intrahepatic biliary tree. Malignant lesions are solid, nodular, and grayish. Most cases are adenocarcinomas. Somatic mutations in BAP1, ARID1A, PBRM1, IDH1, and IDH2 genes have been identified. OMIM: 615619