Table 1.
Disease | Gene |
Wilson disease | Cu-transporting ATPase |
Hereditary hemochromatosis | HFE |
Crigler-Najjar syndrome | UDP-glucuronosyltransferase |
Dubin-Johnson syndrome | cMOAT |
Benign recurrent intrahepatic cholestasis | P-type ATPase |
Progressive familial Intrahepatic Cholestasis Type 1 | P-type ATPase |