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Familial primary hypomagnesemia

MONDO:0018100

A 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.

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Sub-types

EGF-related primary hypomagnesemia with intellectual disability (0) Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis (0) Familial primary hypomagnesemia with hypocalcuria (0) Familial primary hypomagnesemia with normocalciuria and normocalcemia (0) Familial primary hypomagnesemia with normocalcuria (0) Hypomagnesemia 7, renal, with or without dilated cardiomyopathy (0) Hypomagnesemia, seizures, and intellectual disability (0) Hypomagnesemia, seizures, and intellectual disability 1 (0) Hypomagnesemia, seizures, and intellectual disability 2 (0) Intestinal hypomagnesemia 1 (0) Isolated autosomal dominant hypomagnesemia, Glaudemans type (0) Renal hypomagnesemia 2 (0) Renal hypomagnesemia 3 (0) Renal hypomagnesemia 4 (0) Renal hypomagnesemia 5 with ocular involvement (0) Renal hypomagnesemia 6 (0)

Broader categories

Disease (680) Metabolic disease (233) Kidney disorder (214) Hereditary disease (176) Urinary system disorder (66) Inborn errors of metabolism (45) Human disease (14) Disease of genetic or genomic mechanism (2) Inborn metal metabolism disorder (1) Inherited kidney disorder (1)

Trials to join now! 1 Not yet finished but already full! 2 Completed 2