Familial primary hypomagnesemia with normocalcuria
MONDO:0017626Familial primary hypomagnesemia with normocalcuria (FPHN) is a form of familial primary hypomagnesemia (FPH) which is characterized by low magnesium values but normal calcium values in the serum. The disorder consists of three distinct forms which are: autosomal recessive primary hypomagnesemia with normocalcuria and hypocalcemia (ARPHN), familial primary hypomagnesemia with normocalcuria and normocalcemia (FPHNN) and isolated autosomal dominant hypomagnesemia, Glaudemans type.
1 clinical trial for this condition and its sub-types, 0 tagged with Familial primary hypomagnesemia with normocalcuria itself.
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Browse by category →Sub-types of Familial primary hypomagnesemia with normocalcuria
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3 sub-types
- Hypomagnesemia, seizures, and intellectual disability 0 trials Sub-types →
- Renal hypomagnesemia 4 0 trials
- Renal hypomagnesemia 6 0 trials
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Intestinal hypomagnesemia 1 0 trials