183592 Genetic renal tubular disease
309848 Disorder of magnesium transport
377794 group of disorders
93603 Rare renal tubular disease
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34526 Familial primary hypomagnesemia
definition
Familial primary hypomagnesemia (FPH) is a rare mineral absorption and transport disorder characterized by a selective defect in renal or intestinal magnesium (Mg) absorption, resulting in a low Mg concentration in the blood.
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306516 Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
306519 Familial primary hypomagnesemia with hypocalcuria
306522 Familial primary hypomagnesemia with normocalcuria