Rotor syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Rotor syndrome (RT) is a benign, inherited liver disorder characterized by chronic, predominantly conjugated, nonhemolytic hyperbilirubinemia with normal liver histology. (Orphanet Rare Disease Ontology, Orphanet_3111)
External Link http://www.omim.org/entry/237450
Similar Terms
Downloads & Tools

Genes

1 genes associated with the Rotor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SLCO1B1 solute carrier organic anion transporter family, member 1B1