Other major modification was the categorization of AML with myelodysplasia-related gene (MDS) mutations (ASXL1, BCOR, EZH2, RUNX1, SF3B1, SRSF2, STAG2, U2AF1, and ZRSR2) as adverse genetic risk. The gene discussed is RUNX1; the disease is myelodysplastic syndrome.