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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.

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Sub-types

Medium chain acyl-CoA dehydrogenase deficiency (7) Short chain acyl-CoA dehydrogenase deficiency (4) Carnitine-acylcarnitine translocase deficiency (3) 3-hydroxy-3-methylglutaric aciduria (1) 3-hydroxyacyl-CoA dehydrogenase deficiency (1) Beta-ketothiolase deficiency (1) Carnitine palmitoyl transferase 1A deficiency (1) Carnitine palmitoyltransferase II deficiency (1) Disorder of fatty acid oxidation and ketogenesis (1) Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (1) Multiple acyl-CoA dehydrogenase deficiency (1) Systemic primary carnitine deficiency disease (1) Very long chain acyl-CoA dehydrogenase deficiency (1) 3-hydroxy-3-methylglutaryl-CoA synthase deficiency (0) Acyl-CoA dehydrogenase 9 deficiency (0) Acyl-CoA dehydrogenase deficiency (0) Carnitine palmitoyl transferase deficiency (0) 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)

Broader categories

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

Trials to join now! 9 Not yet recruiting 2 Not yet finished but already full! 7 Completed 1