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Other Names for This Condition Carnitine transporter deficiency Carnitine uptake defect Carnitine uptake deficiency CUD Renal carnitine transport defect Systemic carnitine deficiency Additional Information & Resources Genetic Testing Information Genetic and Rare Diseases Information Center Patient Support and Advocacy Resources Clinical Trials Catalog of Genes and Diseases from OMIM Scientific Articles on PubMed References Amat di San Filippo C, Pasquali M, Longo N

The compound acts as a precursor to Nicotinamide Adenine Dinucleotide (NAD+), an essential coenzyme present in all living cells, crucial for metabolic processes and cellular repair

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inositol, a carbocyclic sugar involved in insulin signaling

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