Among these, we identified ten pseudogenes that were associated with skin or hair diseases (ALOX15, AWAT2, EDA2R, FABP4, FLG2, GNLY, MC5R, MOGAT3, NLRP10, and SERPINB12), six (CD96, DCHS2, FAM111A, IGSF23, and LILRB3) with skeletal development and/or bone density, and two (AANAT and MTNR1B) with circadian rhythms (Figures 2D, 2E, and S7). The gene discussed is ALOX15; the disease is disorder of pilosebaceous unit.