The Venn graphic shows the DEGs common to hypothyroidism and OSA (Figure 3E), including AGT, RANBP3L, ACTA2, TCEANC2, FGR, RAMP3, IMPA2, RGS4, PLK3, UCN3, PFKFB3, MARCO, CXCL2, NLRP3, TREM2, TMSB15B, SKA3, OR51E1, ZNF252P, MSTO1, IL1RL1, FAIM, RAB20, EPPIN, CAPNS1, PIGF, CD300LB, NR4A1, NRIP1, PCDHB10, ATF3, NUDT7, MOGS, ZFP36L1, PSMD14, ERRFI1, ENC1, SLC5A3, SLC35G1, HIGD1A, TM4SF18, PTGES3, OR56A4, KIF5C, MMRN1, PLBD2, MCL1, and RPL29. The gene discussed is PCDHB10; the disease is hypothyroidism.