NR3C2 and myalgic encephalomeyelitis/chronic fatigue syndrome: It should be noted that both Goertzel et al. [85] and Rajeevan et al. [86] had previously reported that NR3C1 haplotypes were differentially present in CFS patients while Macedo et al. [87] observed that a related gene SNP for NR3C2, the mineralocorticoid receptor, was differentially present in FMS patients and this was linked to lower baseline gene expression of both NR3C1 and NR3C2.