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Diseases

Biliary Atresia

biliary atresia

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
Biliary Atresia
Standard Disease Name
biliary atresia
MeSH Tree
No data
ICD-10
Q44.2

Identifiers

DO ID
No data
MeSH ID
D001656
OMIM ID
MTHU019102|MTHU049398|MTHU031727|210500
UMLS ID
C0005411
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:A congenital disorder characterized by blockage or absence of the intrahepatic or extrahepatic bile ducts.|NCI2016_02D:A congenital disorder characterized by blockage or absence of the extrahepatic bile ducts.|MSH2017_2016_08_12:Progressive destruction or the absence of all or part of the extrahepatic BILE DUCTS, resulting in the complete obstruction of BILE flow. Usually, biliary atresia is found in infants and accounts for one third of the neonatal cholestatic JAUNDICE.|HPO2016_07_04:Atresia in the extrahepatic bile duct. [HPO:probinson]|HPO2016_07_04:Atresia in of the biliary tree. [HPO:probinson]|CSP2006:progressive destruction or the absence of all or part of the extrahepatic bile ducts, resulting in the complete obstruction of bile flow; found mainly in infants.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
06
ICAM1
intercellular adhesion molecule 1
intercellular adhesion molecule 1
07
IGFBP1
insulin like growth factor binding protein 1
insulin like growth factor binding protein 1
08
PCK1
phosphoenolpyruvate carboxykinase 1
phosphoenolpyruvate carboxykinase 1