Additional evidence from the literature not yet reflected in OMIM or any other database include possibly pathogenic variants described in one or a few families in ZMYM343, GPKOW44, and WNK3. Loss-of-function and missense variants in WNK3 have been identified in six different families with intellectual disability and variable epilepsy in June 2022 during the revision of this article45. Here, WNK3 is linked to Intellectual disability.