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:
Fatty-acid metabolism disorders
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Inborn error
of
lipid metabolism
:
fatty-acid metabolism disorders
Synthesis
Biotinidase deficiency
(BTD)
Degradation
Acyl
transport
Carnitine
CPT1
CPT2
CDSP
CACTD
Adrenoleukodystrophy
(ALD)
Beta
oxidation
General
Acyl CoA dehydrogenase
Short-chain
SCADD
Medium-chain
MCADD
Long-chain 3-hydroxy
LCHAD
Very long-chain
VLCADD
Mitochondrial trifunctional protein deficiency
(MTPD):
Acute fatty liver of pregnancy
Unsaturated
2,4 Dienoyl-CoA reductase deficiency
(DECRD)
Odd chain
Propionic acidemia
(PCC deficiency)
Other
3-hydroxyacyl-coenzyme A dehydrogenase deficiency
(HADHD)
Glutaric acidemia type 2
(MADD)
To
acetyl-CoA
Malonic aciduria
(MCD)
Aldehyde
Sjögren–Larsson syndrome
(SLS)
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