Disorder of fatty acid oxidation and ketogenesis
MONDO:001771316 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)
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)
Glutaric acidemia IIa
(0)
Glutaric acidemia IIb
(0)
Glutaric acidemia IIc
(0)
Long chain acyl-CoA dehydrogenase deficiency
(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)
Broader categories
Disease
(680)
Metabolic disease
(233)
Inherited lipid metabolism disorder
(189)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Inherited fatty acid metabolism disorder
(7)
Disorder of fatty acid and ketone body metabolism
(3)
Disease of genetic or genomic mechanism
(2)
Inborn disorder of energy metabolism
(1)