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Disorder of vitamin and non-protein cofactor absorption and transport

MONDO:0017758

Also known as: disorder of vitamin and non-protein cofactor absorption and transport

10 clinical trials for this condition and its sub-types.

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Sub-types

Thiamine-responsive megaloblastic anemia syndrome (6) Methylmalonic aciduria and homocystinuria type cblC (3) 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) Neurodegenerative syndrome due to cerebral folate transport deficiency (1) Transcobalamin II deficiency (1) Amish lethal microcephaly (0) Childhood encephalopathy due to thiamine pyrophosphokinase deficiency (0) Constitutional megaloblastic anemia with severe neurologic disease (0) Disorder of folate metabolism and transport (0)

Broader categories

Disease (717) Metabolic disease (241) Hereditary disease (188) Inborn errors of metabolism (47) Human disease (15) Disease of genetic or genomic mechanism (2) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0) Disorder of metabolite absorption and transport (0)

Trials to join now! 3 Not yet recruiting 1 Not yet finished but already full! 2 Completed 4