Biliary Hyperplasia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description 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. (Human Phenotype Ontology, HP_0006560)
External Link https://www.disgenet.org/browser/0/1/0/C3686778
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Genes

5 genes associated with the disease Biliary Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CTRC chymotrypsin C (caldecrin)
PRSS1 protease, serine, 1 (trypsin 1)
SMAD7 SMAD family member 7
SPINK1 serine peptidase inhibitor, Kazal type 1