Inborn metal metabolism disorder
MONDO:0004689An 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.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Inborn metal metabolism disorder
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Wilson disease 31 trials
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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
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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
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Menkes disease 5 trials
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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
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Acrodermatitis enteropathica 2 trials
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Atransferrinemia 1 trial
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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
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Sulfite oxidase deficiency due to molybdenum cofactor deficiency 0 trials · 1 incl. sub-types
4 sub-types
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A 1 trial
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B1 0 trials
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B2 0 trials
- Sulfite oxidase deficiency due to molybdenum cofactor deficiency type C 0 trials
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)