OnlineIMD

HK1-related disease

  • Type
    Disease
  • Gene
    • HK1 / Hexokinase 1
      • 10q22.1
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Hexokinase-1
  • Pathway
    • Glycolysis and gluconeogenesis
  • Disease group(s)
    • 3.3        Disorders of glycolysis
  • Child entries
    • HK1-related hemolytic anemia
    • Hereditary motor and sensory neuropathy, Russe type
    • HK1-related retionopathy
    • HK1-related neurodevelopmental disorder