Mutations in the epithelial cell adhesion molecule (EPCAM), myosin Vb (MYO5B), Fork head Box P3 gene (FOXBP3), Tetratricopeptide Repeat Domain 37 (TTC37) (35), and the “immune dysregulation, poly-endocrinopathy, enteropathy, X-linked” syndrome (36) have also been implicated in VEO-IBD. This evidence concerns the gene EPCAM and inflammatory bowel disease.