Intestinal Hypomagnesemia 1

About the Disease
Hypomagnesemia 1, Intestinal, also known as intestinal hypomagnesemia 1, is related to hypomagnesemia 3, renal and hypocalcemia, autosomal dominant 1, and has symptoms including seizures and spasm. An important gene associated with Hypomagnesemia 1, Intestinal is TRPM6 (Transient Receptor Potential Cation Channel Subfamily M Member 6), and among its related pathways/superpathways are Ion channel transport and TRP channels. The drugs Inulin and Proton Pump Inhibitors have been mentioned in the context of this disorder. Affiliated tissues include heart, kidney and skin, and related phenotypes are hypocalcemia and hypomagnesemia

Common Targets
TRPM6

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