Gilbert syndrome

An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice.

Also known as: Gilbert disease, Gilbert syndrome, Gilbert's syndrome, familial cholemia, hyperbilirubinemia type 1, hyperbilirubinemia 1, hyperbilirubinemia, Arias type, hyperbilirubinemia, Gilbert type

0 clinical trials for this condition and its sub-types.