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Herb Integrative Database
Traditional Medicine Data Platform
Diseases

Biliary Atresia

biliary atresia

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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
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.