HLX and acute myeloid leukemia: With regard to the HLX gene, several polymorphisms were associated with the clinical course of Graves’ disease (GD), the expression and secretion of type 1/2 T helper (Th1/Th2) cell line cytokines in neonates after birth, the onset of asthma in children, and the development of treatment-dependent acute myeloid leukemia [16,17,20,21].