Disorder of mineral absorption and transport
MONDO:001776166 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Wilson disease
(26)
Hereditary hemochromatosis
(7)
Menkes disease
(5)
Familial primary hypomagnesemia
(4)
Acrodermatitis enteropathica
(2)
Hemochromatosis type 1
(2)
Occipital horn syndrome
(1)
Aceruloplasminemia
(0)
African iron overload
(0)
Atransferrinemia
(0)
Autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect
(0)
Cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome
(0)
Digenic hemochromatosis
(0)
Disorder of copper metabolism
(0)
Disorder of iron metabolism and transport
(0)
Disorder of magnesium transport
(0)
Disorder of manganese transport
(0)
Disorder of zinc metabolism
(0)
EGF-related primary hypomagnesemia with intellectual disability
(0)
Familial benign copper deficiency
(0)