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These other disorders include VLCAD deficiency, CPT2 deficiency, and carnitine acylcarnitine translocase (CACT) deficiency, mitochondrial trifunctional protein (MTP) deficiency (this includes the primary defect in MTP due to pathogenic variants in the long-chain 3-hydroxyacyl-CoA dehydrogenase subunit encoding gene: HADHA), and urea cycle disorders