In T1DM, some of the terms annotated were related to myelin dysregulation (ARHGEF6, CNP, NADK2, PSAP, SLC25A12) and other neurological disorders, such as Alzheimer’s disease (i.e., POA2, APOC1, APOC3, CNP, GSK3B, PON1, PSAP, SELENBP1) or movement disorders (Table 2). This evidence concerns the gene SLC25A12 and movement disorder.