Inborn metal metabolism disorder

MONDO:0004689

An inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals.

Also known as: metal metabolism disorder, metal metabolism, inborn error

60 clinical trials for this condition and its sub-types, 1 tagged with Inborn metal metabolism disorder itself.

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Where it sits in the disease tree

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Part of

↑ Inborn errors of metabolism (2231)

Sub-types of Inborn metal metabolism disorder

Wilson disease 31 trials
Pseudohypoparathyroidism 8 trials · 9 incl. sub-types
5 sub-types
- Pseudohypoparathyroidism type 1A 7 trials
- Pseudopseudohypoparathyroidism 2 trials
- Pseudohypoparathyroidism type 1B 0 trials
- Pseudohypoparathyroidism type 1C 0 trials
- Pseudohypoparathyroidism type 2 0 trials
Hereditary hemochromatosis 8 trials
8 sub-types
- Hemochromatosis type 1 3 trials
- African iron overload 0 trials
- Digenic hemochromatosis 0 trials
- Hemochromatosis type 2 0 trials Sub-types →
- Hemochromatosis type 3 0 trials
- Hemochromatosis type 4 0 trials
- Hemochromatosis type 5 0 trials
- Neonatal hemochromatosis 0 trials
Menkes disease 5 trials
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
Acrodermatitis enteropathica 2 trials
Atransferrinemia 1 trial
Familial periodic paralysis 0 trials · 1 incl. sub-types
6 sub-types
- Hyperkalemic periodic paralysis 1 trial
- Hypokalemic periodic paralysis 1 trial Sub-types →
- Andersen-Tawil syndrome 0 trials
- Normokalemic periodic paralysis 0 trials
- Periodic paralysis with later-onset distal motor neuropathy 0 trials
- Thyrotoxic periodic paralysis 0 trials
Sulfite oxidase deficiency due to molybdenum cofactor deficiency 0 trials · 1 incl. sub-types
4 sub-types

Most studied deeper sub-types

Renal hypomagnesemia 3 (1) Familial primary hypomagnesemia with normocalciuria and normocalcemia (0) Hemochromatosis type 2A (0) Hemochromatosis type 2B (0) Hypokalemic periodic paralysis, type 1 (0) Hypokalemic periodic paralysis, type 2 (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)

Including sub-types (60) Tagged with Inborn metal metabolism disorder (1)

Trials to join now! 19 Not yet recruiting 6 Not yet finished but already full! 19 Completed 13 Terminated 3

Inborn metal metabolism disorder

Where it sits in the disease tree

Most studied deeper sub-types

Slower magnesium drip may help sickest patients hold onto the mineral

New dialysis device for Wilson's disease tested but trial stopped early

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