Disease: HYPERBILIRUBINEMIA, ROTOR TYPE, DIGENIC ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4016905
Disease: HYPERBILIRUBINEMIA, ROTOR TYPE, DIGENIC
HYPERBILIRUBINEMIA, ROTOR TYPE, DIGENIC 		0.300 Biomarker phenotype GENOMICS_ENGLAND Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver. 22232210 2012