OnlineIMD

Carnitine palmitoyltransferase 1A deficiency

(CPT1 deficiency)
  • Type
    Disease
  • External link(s)
    • Orphanet
    • IEMbase
    • VMH
  • Gene
    • CPT1A / Carnitine Palmitoyltransferase 1A
      • 11q13.3
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Carnitine palmitoyltransferase I, liver isoform
  • Pathway
    • Carnitine metabolism and fatty acid oxidation
  • Disease group(s)
    • 4.1        Disorders of carnitine metabolism