Inborn organic aciduria

MONDO:0000688

An inherited disorder that affects the metabolism of any acidic compound containing carbon in a covalent linkage.

Also known as: disorder of organic acid metabolism, organic acid metabolism disorder, inborn error of organic acid metabolic process, inborn organic acid metabolic process disorder, organic acidemia, organic aciduria, rare inborn error of organic acid metabolic process, inherited organic acidemia

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

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Sub-types

Propionic acidemia (8) Methylmalonic acidemia (7) Barth syndrome (5) Glutaryl-CoA dehydrogenase deficiency (4) Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency (4) Biotinidase deficiency (3) Methylmalonic aciduria and homocystinuria type cblC (3) Isovaleric acidemia (2) Maple syrup urine disease (2) Methylmalonic aciduria and homocystinuria type cblD (2) Methylmalonic aciduria, cblA type (2) 3-hydroxy-3-methylglutaric aciduria (1) 3-methylcrotonyl-CoA carboxylase 1 deficiency (1) 3-methylcrotonyl-CoA carboxylase 2 deficiency (1) Beta-ketothiolase deficiency (1) Holocarboxylase synthetase deficiency (1) Maple syrup urine disease type 1A (1) Maple syrup urine disease type 1B (1) Maple syrup urine disease type 2 (1) Methylmalonic acidemia with homocystinuria, type cblJ (1)

Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Inborn errors of metabolism (45) Human disease (14) Inborn disorder of amino acid metabolism (4) Disease of genetic or genomic mechanism (2) Amino acid metabolism disease (1) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0)

Trials to join now! 19 Not yet recruiting 2 Not yet finished but already full! 2 Completed 5 Terminated 1

Inborn organic aciduria

Sub-types

Broader categories

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