SRY translocations, CNVs of FGF9, NR0B1, NR2F2, SOX3, SOX9, SOX10, and SPRY2, and sequence variants of NR5A1, NR2F2, RSPO1, SOX9, WNT4, WNT2B, and WT1 are responsible for the genetic mechanisms associated with 46,XX T/OT-DSD (62). Here, NR0B1 is linked to disorder of sexual differentiation.