Inherited fatty acid metabolism disorder
MONDO:0037858A group of genetic disorders that result from the inability to produce or use an enzyme required to oxidize fatty acids, resulting in an inability to generate energy from fatty acid sources.
Also known as: disorder of fatty acid metabolism, fatty acid metabolism disorder, inherited fatty acid metabolism disorder, disorder of fat oxidation, disorders of fatty-acid metabolism
21 clinical trials for this condition and its sub-types, 7 tagged with Inherited fatty acid metabolism disorder itself.
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Sub-types of Inherited fatty acid metabolism disorder
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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
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Inherited lipoic acid biosynthesis defect 0 trials · 1 incl. sub-types
6 sub-types
- Pyruvate dehydrogenase E3 deficiency 1 trial
- Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities 0 trials
- Fatal multiple mitochondrial dysfunctions syndrome 0 trials Sub-types →
- Lipoic acid synthetase deficiency 0 trials
- Lipoyl transferase 1 deficiency 0 trials
- Spasticity-ataxia-gait anomalies syndrome 0 trials
Most studied deeper sub-types
Medium chain acyl-CoA dehydrogenase deficiency
(7)
Short chain acyl-CoA dehydrogenase deficiency
(4)
Multiple acyl-CoA dehydrogenase deficiency
(1)
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)
Multiple mitochondrial dysfunctions syndrome 1
(0)
Multiple mitochondrial dysfunctions syndrome 10
(0)
Multiple mitochondrial dysfunctions syndrome 2
(0)
Multiple mitochondrial dysfunctions syndrome 3
(0)
Multiple mitochondrial dysfunctions syndrome 4
(0)
Multiple mitochondrial dysfunctions syndrome 5
(0)
Multiple mitochondrial dysfunctions syndrome 6
(0)
Multiple mitochondrial dysfunctions syndrome 7
(0)
Multiple mitochondrial dysfunctions syndrome 9b
(0)
Transient neonatal multiple acyl-CoA dehydrogenase deficiency
(0)