Disorder of metabolite absorption and transport
MONDO:001775759 clinical trials for this condition and its sub-types, 0 tagged with Disorder of metabolite absorption and transport itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Disorder of metabolite absorption and transport
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Disorder of mineral absorption and transport 0 trials · 50 incl. sub-types
5 sub-types
- Disorder of copper metabolism 0 trials · 35 incl. sub-types Sub-types →
- Disorder of iron metabolism and transport 0 trials · 9 incl. sub-types Sub-types →
- Disorder of magnesium transport 0 trials · 5 incl. sub-types Sub-types →
- Disorder of zinc metabolism 0 trials · 2 incl. sub-types Sub-types →
- Disorder of manganese transport 0 trials Sub-types →
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Disorder of vitamin and non-protein cofactor absorption and transport 0 trials · 10 incl. sub-types
4 sub-types
- Disorder of thiamine metabolism and transport 0 trials · 7 incl. sub-types Sub-types →
- Inborn disorder of cobalamin metabolism and transport 1 trial · 3 incl. sub-types Sub-types →
- Disorder of folate metabolism and transport 0 trials · 2 incl. sub-types Sub-types →
- Hereditary hypercarotenemia and vitamin A deficiency 0 trials Sub-types →
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Maternal riboflavin deficiency 0 trials
Most studied deeper sub-types
Wilson disease
(31)
Hereditary hemochromatosis
(8)
Thiamine-responsive megaloblastic anemia syndrome
(6)
Familial primary hypomagnesemia
(5)
Menkes disease
(5)
Hemochromatosis type 1
(3)
Methylmalonic aciduria and homocystinuria type cblC
(3)
Acrodermatitis enteropathica
(2)
Methylcobalamin deficiency type cblE
(2)
Methylcobalamin deficiency type cblG
(2)
Methylmalonic aciduria and homocystinuria type cblD
(2)
Methylmalonic aciduria, cblA type
(2)
Atransferrinemia
(1)
Biotin-responsive basal ganglia disease
(1)
Hereditary intrinsic factor deficiency
(1)
Homocystinuria due to methylene tetrahydrofolate reductase deficiency
(1)
Methylmalonic acidemia with homocystinuria, type cblJ
(1)
Methylmalonic aciduria and homocystinuria
(1)
Methylmalonic aciduria and homocystinuria type cblF
(1)
Methylmalonic aciduria, cblB type
(1)
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