Clinical manifestations of our G6PD-deficient children were classified as 91 individuals (89.2%) with neonatal hyperbilirubinemia (66 males and 25 females) and 11 individuals (10.8%) with acute hemolytic anemia (7 males and 4 females) (Table 1). The gene discussed is G6PD; the disease is Hyperbilirubinemia.