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, 5 tagged with Inborn organic aciduria itself.

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Where it sits in the disease tree

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Part of

↑ Inborn disorder of amino acid metabolism (159)

Sub-types of Inborn organic aciduria

Classic organic aciduria 0 trials · 20 incl. sub-types
15 sub-types
- Propionic acidemia 8 trials Sub-types →
- 3-methylglutaconic aciduria 0 trials · 5 incl. sub-types Sub-types →
- Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency 4 trials Sub-types →
- Methylmalonic aciduria and homocystinuria 1 trial · 3 incl. sub-types Sub-types →
- Multiple carboxylase deficiency 0 trials · 3 incl. sub-types Sub-types →
- Isovaleric acidemia 2 trials
- Vitamin B12-responsive methylmalonic acidemia 0 trials · 2 incl. sub-types Sub-types →
- 3-hydroxy-3-methylglutaric aciduria 1 trial
- 3-methylcrotonyl-CoA carboxylase deficiency 0 trials · 1 incl. sub-types Sub-types →
- Beta-ketothiolase deficiency 1 trial
- 2-methylbutyryl-CoA dehydrogenase deficiency 0 trials
- 3-hydroxyisobutyric aciduria 0 trials
- 3-hydroxyisobutyryl-CoA hydrolase deficiency 0 trials
- Combined malonic and methylmalonic acidemia 0 trials
- Isobutyryl-CoA dehydrogenase deficiency 0 trials
Methylmalonic acidemia 7 trials · 8 incl. sub-types
7 sub-types
- Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency 4 trials Sub-types →
- Methylmalonic aciduria and homocystinuria 1 trial · 3 incl. sub-types Sub-types →
- Vitamin B12-responsive methylmalonic acidemia 0 trials · 2 incl. sub-types Sub-types →
- Combined malonic and methylmalonic acidemia 0 trials
- Isolated methylmalonic aciduria cblD type 0 trials
- Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency 0 trials
- Methylmalonic acidemia due to transcobalamin receptor defect 0 trials
Glutaryl-CoA dehydrogenase deficiency 4 trials
Maple syrup urine disease 2 trials · 4 incl. sub-types
9 sub-types
- Maple syrup urine disease type 1A 1 trial
- Maple syrup urine disease type 1B 1 trial
- Maple syrup urine disease type 2 1 trial
- Pyruvate dehydrogenase E3 deficiency 1 trial
- Classic maple syrup urine disease 0 trials
- Intermediate maple syrup urine disease 0 trials
- Intermittent maple syrup urine disease 0 trials
- Maple syrup urine disease, mild variant 0 trials
- Thiamine-responsive maple syrup urine disease 0 trials
Glutaric acidemia type 3 0 trials
Malonic aciduria 0 trials
Methylmalonate semialdehyde dehydrogenase deficiency 0 trials

Most studied deeper sub-types

Including sub-types (29) Tagged with Inborn organic aciduria (5)

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

Inborn organic aciduria

Where it sits in the disease tree

Most studied deeper sub-types

Could a vitamin B12 shot help kids with MMA? new trial underway

Could a breath test replace blood draws for metabolic disease monitoring?