dubin-johnson syndrome Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin without elevation of liver alanine transaminase and aspartate transaminase enzymes as a result of the deficient ability of hepatocytes to secrete conjugated bilirubin into the bile. (Human Disease Ontology, DOID_12308)
Similar Terms
Downloads & Tools

Genes

1 genes involed in the disease dubin-johnson syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCC2 ATP-binding cassette, sub-family C (CFTR/MRP), member 2