For example, genes associated with neurodevelopmental disorders (ALS2, ATP8A2, FA2H, FGD4, HTRA2, SNAP29, VLDLR, VRK1, WDR81) and rare diseases (ALX1, BBS10, CHST14, DDR2, SLC34A2, TAC3, TACR3) have been identified in Mediterranean and Middle Eastern families. Here, ALX1 is linked to neurodevelopmental disorder.