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Up to: Inborn metal metabolism disorder · Inherited renal tubular disease · Disorder of magnesium transport

Familial primary hypomagnesemia

A hereditary disorder that leads to a selective defect in renal or intestinal magnesium absorption, resulting in a low serum magnesium concentration.

5 trials tagged with this condition →

  • Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis 0 trials · 1 incl. sub-types Sub-types →
  • EGF-related primary hypomagnesemia with intellectual disability 0 trials
  • Familial primary hypomagnesemia with hypocalcuria 0 trials Sub-types →
  • Familial primary hypomagnesemia with normocalcuria 0 trials Sub-types →
  • Hypomagnesemia 7, renal, with or without dilated cardiomyopathy 0 trials

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