OnlineIMD

Pyruvate carboxylase deficiency

(PC deficiency)
  • Type
    Disease
  • External link(s)
    • Orphanet
    • IEMbase
    • VMH
  • Gene
    • PC / Pyruvate Carboxylase
      • 11q13.2
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Pyruvate carboxylase
  • Pathway
    • Glycolysis and gluconeogenesis
  • Disease group(s)
    • 3.2        Disorders of gluconeogenesis
  • Child entries
    • Pyruvate carboxylase deficiency, severe neonatal type
    • Pyruvate carboxylase deficiency, infantile type
    • Pyruvate carboxylase deficiency, benign type