bilirubin metabolic disorder Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism. (Human Disease Ontology, DOID_2741)
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Genes

2 genes involed in the disease bilirubin metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCC2 ATP-binding cassette, sub-family C (CFTR/MRP), member 2
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1