Human Phenotype Ontology 
Grandparent Node:
expandBiliary tract abnormality (HP:0001080)help
Parent Node:
expandAbnormal biliary tract morphology (HP:0012440)help
..Starting node
..expandBiliary hyperplasia (HP:0006560)help
Term ID: 6560
Name: Biliary hyperplasia
Synonym: Bile duct hyperplasia
Definition: Hyperplasia of the biliary tree, as manifested by increased size of bile ducts, dilated lumen, and histologically by an increased number of epithelial cells or hyperplasia.
Comments:
Reference: HP:0006560
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal intrahepatic bile duct morphology (HP:0011040) help
..expandAbnormality of the ductus choledochus (HP:0100889) help
..expandBile duct proliferation (HP:0001408) help
..expandBiliary atresia (HP:0005912) help
..expandBiliary cirrhosis (HP:0002613) help
..expandBiliary epithelial hyperplasia (HP:0030986) help
..expandBiliary tract neoplasm (HP:0100574) help
..expandBiliary tract obstruction (HP:0005230) help
..expandCholangitis (HP:0030151) help
..expandPortosystemic collateral veins (HP:0025154) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006560HP:0006560Biliary hyperplasia0DZIP1L CL E G H19922126551ORPHA:731Autosomal recessive polycystic kidney diseaseHP:0040282 - Frequent4
HP:0006560HP:0006560Biliary hyperplasia0FOCAD CL E G H5491423377OMIM:6199913
HP:0006560HP:0006560Biliary hyperplasia0PKHD1 CL E G H53149016ORPHA:731Autosomal recessive polycystic kidney diseaseHP:0040282 - Frequent563


Genes (3) :DZIP1L FOCAD PKHD1

Diseases (2) :ORPHA:731 OMIM:619991
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.