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Disorder of fatty acid and ketone body metabolism

MONDO:0019223

Also known as: inborn disorder of fatty acid oxidation and ketone body metabolism, disorder of fatty acid oxidation and ketone body metabolism

19 clinical trials for this condition and its sub-types, 3 tagged with Disorder of fatty acid and ketone body metabolism itself.

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Where it sits in the disease tree

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Part of

↑ Inborn disorder of energy metabolism (235)

Sub-types of Disorder of fatty acid and ketone body metabolism

Disorder of fatty acid oxidation and ketogenesis 1 trial · 16 incl. sub-types
10 sub-types
- Acyl-CoA dehydrogenase deficiency 0 trials · 12 incl. sub-types Sub-types →
- Carnitine-acylcarnitine translocase deficiency 3 trials
- 3-hydroxy-3-methylglutaric aciduria 1 trial
- 3-hydroxyacyl-CoA dehydrogenase deficiency 1 trial
- Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency 1 trial
- Systemic primary carnitine deficiency disease 1 trial
- Very long chain acyl-CoA dehydrogenase deficiency 1 trial
- 3-hydroxy-3-methylglutaryl-CoA synthase deficiency 0 trials
- Acyl-CoA dehydrogenase 9 deficiency 0 trials
- Long chain acyl-CoA dehydrogenase deficiency 0 trials
Disorder of carnitine cycle and carnitine transport 0 trials · 4 incl. sub-types
3 sub-types
- Carnitine-acylcarnitine translocase deficiency 3 trials
- Carnitine palmitoyl transferase deficiency 0 trials · 1 incl. sub-types Sub-types →
- Systemic primary carnitine deficiency disease 1 trial
Inborn disorder of ketolysis 0 trials · 1 incl. sub-types
2 sub-types
- Beta-ketothiolase deficiency 1 trial
- Succinyl-CoA:3-ketoacid CoA transferase deficiency 0 trials
Ketoacidosis due to monocarboxylate transporter-1 deficiency 0 trials

Most studied deeper sub-types

Medium chain acyl-CoA dehydrogenase deficiency (7) Short chain acyl-CoA dehydrogenase deficiency (4) Carnitine palmitoyl transferase 1A deficiency (1) Carnitine palmitoyltransferase II deficiency (1) Multiple acyl-CoA dehydrogenase deficiency (1) Carnitine palmitoyl transferase II deficiency, myopathic form (0) Carnitine palmitoyl transferase II deficiency, neonatal form (0) Carnitine palmitoyl transferase II deficiency, severe infantile form (0) Glutaric acidemia IIa (0) Glutaric acidemia IIb (0) Glutaric acidemia IIc (0) Multiple acyl-CoA dehydrogenase deficiency, mild type (0) Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type (0) Transient neonatal multiple acyl-CoA dehydrogenase deficiency (0)

Including sub-types (19) Tagged with Disorder of fatty acid and ketone body metabolism (3)

Trials to join now! 2 Not yet finished but already full! 1