Disorder of magnesium transport
MONDO:0017765An inherited metabolic disease that is has its basis in the disruption of magnesium ion transport.
Also known as: inborn error of magnesium ion transport, inborn magnesium ion transport disorder, rare inborn error of magnesium ion transport
5 clinical trials for this condition and its sub-types, 0 tagged with Disorder of magnesium transport itself.
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Browse by category →Sub-types of Disorder of magnesium transport
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Familial primary hypomagnesemia 5 trials
5 sub-types
- Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis 0 trials · 1 incl. sub-types Sub-types →
- EGF-related primary hypomagnesemia with intellectual disability 0 trials
- Familial primary hypomagnesemia with hypocalcuria 0 trials Sub-types →
- Familial primary hypomagnesemia with normocalcuria 0 trials Sub-types →
- Hypomagnesemia 7, renal, with or without dilated cardiomyopathy 0 trials
Most studied deeper sub-types
Renal hypomagnesemia 3
(1)
Familial primary hypomagnesemia with normocalciuria and normocalcemia
(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 4
(0)
Renal hypomagnesemia 5 with ocular involvement
(0)
Renal hypomagnesemia 6
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.