Neurological Disorder (8.5 × 10-3-4.8 × 10-2) involved the following genes: ACADM, AP1S2, ATP6AP2, B2M, CAB39, CDKN1B, CHMP2B, CRBN, DDX1, EIF3E, GALC, GHITM, GNA13, HMGB2, HMGCR, HSP90AA1, IFNGR1, IMPA1, ITPR1, IVNS1ABP, L1CAM, NDUFB5, NFE2L2, OSBPL8, PCMT1, PPP1CB, PPP1R2, PRNP, PTGS2, RAB1A, RAB11A, RAB3GAP2, RAB5A, SLC9A6 TOMM20 and TRAM1. The gene discussed is HMGB2; the disease is nervous system disorder.