The top categories from the “Diseases and Bio Functions Analysis” included “Transport of molecule,” “Morphology of head,” “Glycolysis of cell,” “Morphology of nervous system,” and “Familial hemolytic anemia” — all of which confirms the data presented herein — as well as the associations of human SLC39A8 variants with most if not all of the clinical disorders (vide supra). Here, SLC39A8 is linked to familial hemolytic anemia.