Hypomagnesemia 6, Renal, also known as renal hypomagnesemia 6, is related to jalili syndrome and bartter syndrome, type 3, and has symptoms including headache, vertigo and muscle weakness. An important gene associated with Hypomagnesemia 6, Renal is CNNM2 (Cyclin And CBS Domain Divalent Metal Cation Transport Mediator 2). Related phenotypes are hypomagnesemia and impaired renal tubular reabsorption of magnesium