Disorder of metabolite absorption and transport
MONDO:001775774 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)
Thiamine-responsive megaloblastic anemia syndrome
(5)
Familial primary hypomagnesemia
(4)
Methylmalonic aciduria and homocystinuria type cblC
(3)
Acrodermatitis enteropathica
(2)
Hemochromatosis type 1
(2)
Methylcobalamin deficiency type cblE
(2)
Methylcobalamin deficiency type cblG
(2)
Methylmalonic aciduria and homocystinuria type cblD
(2)
Methylmalonic aciduria, cblA type
(2)
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)
Neurodegenerative syndrome due to cerebral folate transport deficiency
(1)