OnlineIMD

Very long-chain acyl-CoA dehydrogenase deficiency

(LCAD deficiency)
  • Type
    Disease
  • External link(s)
    • Orphanet
    • IEMbase
    • VMH
  • Gene
    • ACADVL / Acyl-CoA Dehydrogenase Very Long Chain
      • 17p13.1
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Very long-chain specific acyl-CoA dehydrogenase, mitochondrial
  • Pathway
    • Carnitine metabolism and fatty acid oxidation
  • Disease group(s)
    • 4.2        Disorders of mitochondrial fatty acid oxidation