Mineral metabolism disease
MONDO:0000226Also known as: disease of mineral metabolism, disorder of mineral metabolism
137 clinical trials for this condition and its sub-types, 2 tagged with Mineral metabolism disease itself.
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Sub-types of Mineral metabolism disease
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Calcium metabolic disease 5 trials · 62 incl. sub-types
4 sub-types
- Calcinosis 30 trials · 47 incl. sub-types Sub-types →
- Autosomal dominant hypocalcemia 9 trials · 10 incl. sub-types Sub-types →
- Hypercalcemia disease 4 trials · 7 incl. sub-types Sub-types →
- Calcium-alkali syndrome 0 trials
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Phosphorus metabolism disease 1 trial · 33 incl. sub-types
2 sub-types
- Hyperphosphatemia 22 trials
- Hypophosphatemia 12 trials
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Iron metabolism disease 2 trials · 22 incl. sub-types
2 sub-types
- Hemosiderosis 2 trials · 12 incl. sub-types Sub-types →
- Neurodegeneration with brain iron accumulation 1 trial · 8 incl. sub-types Sub-types →
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Sulfur metabolism disease 0 trials · 14 incl. sub-types
4 sub-types
- Inborn disorder of methionine cycle and sulfur amino acid metabolism 0 trials · 11 incl. sub-types Sub-types →
- Biotin metabolic disease 0 trials · 3 incl. sub-types Sub-types →
- Inherited glutathione metabolism disease 0 trials · 1 incl. sub-types Sub-types →
- Inherited lipoic acid biosynthesis defect 0 trials · 1 incl. sub-types Sub-types →
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Potassium deficiency disease 4 trials · 5 incl. sub-types
1 sub-type
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Diastrophic dysplasia 2 trials
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Achondrogenesis type IB 0 trials
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Acquired mineral metabolism disease 0 trials
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Atelosteogenesis type II 0 trials
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Multiple epiphyseal dysplasia type 4 0 trials
Most studied deeper sub-types
Calciphylaxis
(9)
Hereditary hemochromatosis
(8)
Homocystinuria
(7)
Nephrocalcinosis
(7)
Autosomal dominant hypocalcemia 1
(4)
Classic homocystinuria
(4)
Neurodegeneration with brain iron accumulation 5
(4)
Pantothenate kinase-associated neurodegeneration
(4)
Biotinidase deficiency
(3)
Hemochromatosis type 1
(3)
Hyperhomocysteinemia
(3)
Methylmalonic aciduria and homocystinuria type cblC
(3)
Hypercalcemia, infantile
(2)
Methylcobalamin deficiency type cblE
(2)
Methylcobalamin deficiency type cblG
(2)
Methylmalonic aciduria and homocystinuria type cblD
(2)
Pulmonary hemosiderosis
(2)
Autosomal dominant hypocalcemia 2
(1)
Familial hypocalciuric hypercalcemia 1
(1)
Familial tumoral calcinosis
(1)