People with this disorder have a faulty enzyme, Carnitine palmitoyltransferase I, that prevents these long-chain fatty acids from being transported into the mitochondria to be broken down.
Glucose-6-phosphate dehydrogenase deficiency | Ribose-5-phosphate isomerase deficiency | Phosphorus deficiency | Nitrogen deficiency | Lipoprotein lipase deficiency | Iron deficiency (medicine) | Iron deficiency | Holocarboxylase synthetase deficiency | Growth hormone deficiency | Carnitine palmitoyltransferase I |