The generation of beta-thalassemia (β-Thal) patient-specific induced pluripotent stem cells (iPSCs), subsequent homologous recombination-based gene correction of disease-causing mutations/deletions in the β-globin gene (HBB) and their derived hematopoietic stem cells (HSCs) transplantation offers an ideal therapeutic solution for treating this disease. However, the hematopoietic differentiation efficiency of gene-corrected β-Thal iPSCs has not been well evaluated in the previous studies. In this study, we used the latest gene-editing tool CRISPR/Cas9 to correct β-Thal iPSCs, gene-corrected cells exhibit normal karyotypes and fully pluripotency as hES, showed no off-targeting effects. Then we evaluated the differentiation efficiency of the gene corrected β-Thal iPSCs. We found that during hematopoietic differentiation, gene-corrected β-Thal iPSCs showed increased embryoid body (EB) ratio and various hematopoietic progenitor cells percentages. More importantly, the gene-corrected β-Thal iPS cell lines restored HBB expression and reduced reactive oxygen species (ROS) production compared to un-corrected group. Our study suggested that hematopoietic differentiation efficiency of β-Thal iPSCs were greatly improved once corrected by CRISPR/Cas9 system. And the information gained from our study would greatly promote the clinical application of β-Thal iPSCs-derived HSCs in transplantation.