Familial primary hypomagnesemia
MONDO:0018100A hereditary disorder that leads to a selective defect in renal or intestinal magnesium absorption, resulting in a low serum magnesium concentration.
Also known as: hypomagnesemia, familial primary hypomagnesemia
6 clinical trials for this condition and its sub-types, 5 tagged with Familial primary hypomagnesemia itself.
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Sub-types of Familial primary hypomagnesemia
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Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis 0 trials · 1 incl. sub-types
2 sub-types
- Renal hypomagnesemia 3 1 trial
- Renal hypomagnesemia 5 with ocular involvement 0 trials
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1 sub-type
- Renal hypomagnesemia 2 0 trials
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3 sub-types