A similar outcome was seen with mutations in the gene encoding the related enzyme β-1,3-galactosyltransferase 6 (B3GALT6), which causes Ehlers–Danlos syndrome, spondylodysplastic type 2 (EDSSPD2) and spondyloepimetaphysical dyspasia with joint laxity 1 (SEMDJL1) (Malfait et al., 2013; Nakajima et al., 2013; Van Damme et al., 2018; Vorster et al., 2015). The gene discussed is B3GALT6; the disease is Ehlers-Danlos syndrome, spondylodysplastic type, 2.