Disorder of fatty acid and ketone body metabolism
MONDO:0019223Also 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.
Follow this condition — get notified about new trialsSub-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)