Disorder of metabolite absorption and transport
MONDO:001775756 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Wilson disease
(30)
Hereditary hemochromatosis
(8)
Thiamine-responsive megaloblastic anemia syndrome
(6)
Menkes disease
(5)
Familial primary hypomagnesemia
(4)
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)
Biotin-responsive basal ganglia disease
(1)
Hereditary intrinsic factor deficiency
(1)
Homocystinuria due to methylene tetrahydrofolate reductase deficiency
(1)
Inborn disorder of cobalamin metabolism and transport
(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)