|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the Rotor syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|SLCO1B1||solute carrier organic anion transporter family, member 1B1|