Neonatal intrahepatic cholestasis due to citrin deficiency is a mild subtype of citrin deficiency characterized clinically by low birth weight, failure to thrive, transient intrahepatic cholestasis, multiple aminoacidemia, galactosemia, hypoproteinemia, hepatomegaly, decreased coagulation factors, hemolytic anemia, variable but mostly mild liver dysfunction, and hypoglycemia. The disease is Monarch Disease Ontology identifier MONDO_0011601 (neonatal intrahepatic cholestasis due to citrin deficiency). Also known as: NICCD, neonatal intrahepatic cholestasis caused by citrin deficiency.