Congenital disorder of glycosylation with hepatic involvement +
dicrocoeliasis
FTH1-related iron overload
gallbladder disease +
Glycogen storage disease due to glucose-6-phosphatase deficiency +
hepatic failure, early-onset, and neurologic disorder due to cytochrome c oxidase deficiency
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1
Intrahepatic cholestasis of pregnancy
Intrahepatic cholestasis of pregnancy (ICP) is a cholestatic disorder characterized by (i) pruritus with onset in the second or third trimester of pregnancy, (ii) elevated serum aminotransferases and bile acid levels, and (iii) spontaneous relief of signs and symptoms within two to three weeks after delivery.