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Diseases
Intrahepatic Cholangiocarcinoma
intrahepatic cholangiocarcinoma
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
Grouped by core information, identifiers, and descriptions.
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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