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
5 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
EGF-related primary hypomagnesemia with intellectual disability
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Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis
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Familial primary hypomagnesemia with hypocalcuria
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Familial primary hypomagnesemia with normocalciuria and normocalcemia
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Familial primary hypomagnesemia with normocalcuria
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Hypomagnesemia 7, renal, with or without dilated cardiomyopathy
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Hypomagnesemia, seizures, and intellectual disability
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Hypomagnesemia, seizures, and intellectual disability 1
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Hypomagnesemia, seizures, and intellectual disability 2
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Intestinal hypomagnesemia 1
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Isolated autosomal dominant hypomagnesemia, Glaudemans type
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Renal hypomagnesemia 2
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Renal hypomagnesemia 3
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Renal hypomagnesemia 4
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Renal hypomagnesemia 5 with ocular involvement
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Renal hypomagnesemia 6
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