Previous research [47] in Han Chinese NTD pedigrees showed that genes with hypermethylations clustered in pathways associated with epithelial-to-mesenchymal transition (ZEB2, SMAD6, and CDH23) and folic acid/homocysteine metabolism (MTHFD1L), although significant differences were not detected in our results. The gene discussed is MTHFD1L; the disease is neural tube defect.