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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

6 clinical trials for this condition and its sub-types, 5 tagged with Familial primary hypomagnesemia itself.

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Where it sits in the disease tree

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Part of

↑ Inborn metal metabolism disorder (60) ↑ Inherited renal tubular disease (40) ↑ Disorder of magnesium transport (5)

Sub-types of Familial primary hypomagnesemia

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
EGF-related primary hypomagnesemia with intellectual disability 0 trials
Familial primary hypomagnesemia with hypocalcuria 0 trials
1 sub-type
- Renal hypomagnesemia 2 0 trials
Familial primary hypomagnesemia with normocalcuria 0 trials
3 sub-types
- Familial primary hypomagnesemia with normocalciuria and normocalcemia 0 trials Sub-types →
- Intestinal hypomagnesemia 1 0 trials
- Isolated autosomal dominant hypomagnesemia, Glaudemans type 0 trials
Hypomagnesemia 7, renal, with or without dilated cardiomyopathy 0 trials

Most studied deeper sub-types

Hypomagnesemia, seizures, and intellectual disability (0) Hypomagnesemia, seizures, and intellectual disability 1 (0) Hypomagnesemia, seizures, and intellectual disability 2 (0) Renal hypomagnesemia 4 (0) Renal hypomagnesemia 6 (0)

Including sub-types (6) Tagged with Familial primary hypomagnesemia (5)

Not yet finished but already full! 2 Completed 2 Terminated 1