Gilbert’s syndrome is a chronic familial non-hemolytic jaundice, a congenital genetic disorder, in which patients generally have no obvious clinical symptoms, and some patients sometimes experience liver discomfort, fatigue, and indigestion. The most common feature is a mild increase in indirect bilirubin in the blood, which is usually triggered or aggravated by exertion, hunger, infection, fever, etc., or alcohol consumption, and sometimes accompanied by mild hemolytic anemia. Therefore, to find out if you have Gilbert’s syndrome, you can do tests and examinations.