Disorder of glycolysis

Part of

Sub-types of Disorder of glycolysis

• Maturity-onset diabetes of the young 8 trials · 13 incl. sub-types
  15 sub-types

  • Maturity-onset diabetes of the young type 2 4 trials
  • Maturity-onset diabetes of the young type 1 1 trial
  • Maturity-onset diabetes of the young type 4 1 trial
  • Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young 0 trials
  • Maturity-onset diabetes of the young type 10 0 trials
  • Maturity-onset diabetes of the young type 11 0 trials
  • Maturity-onset diabetes of the young type 13 0 trials
  • Maturity-onset diabetes of the young type 14 0 trials
  • Maturity-onset diabetes of the young type 3 0 trials
  • Maturity-onset diabetes of the young type 6 0 trials
  • Maturity-onset diabetes of the young type 7 0 trials
  • Maturity-onset diabetes of the young type 8 0 trials
  • Maturity-onset diabetes of the young type 9 0 trials
  • Maturity-onset diabetes of the young, type 12 0 trials
  • Renal cysts and diabetes syndrome 0 trials
• Pyruvate kinase deficiency of red cells 10 trials
• Permanent neonatal diabetes mellitus 2 trials
  5 sub-types

  • DEND syndrome 0 trials Sub-types →
  • Diabetes mellitus, permanent neonatal 2 0 trials
  • Diabetes mellitus, permanent neonatal 3 0 trials
  • Diabetes mellitus, permanent neonatal 4 0 trials
  • Permanent neonatal diabetes mellitus 1 0 trials
• Glycogen storage disease VII 1 trial
• Glycogen storage disease due to aldolase A deficiency 1 trial
• Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency 1 trial
• Glycogen storage disease due to muscle beta-enolase deficiency 1 trial
• Glycogen storage disease due to phosphoglycerate mutase deficiency 1 trial
• Charcot-Marie-Tooth disease type 4G 0 trials
• Glycogen storage disease due to lactate dehydrogenase H-subunit deficiency 0 trials
• Glycogen storage disease due to phosphoglycerate kinase 1 deficiency 0 trials
• Hemolytic anemia due to glucophosphate isomerase deficiency 0 trials
• Hyperinsulinemic hypoglycemia, familial, 3 0 trials
• Lactic aciduria due to D-lactic acid 0 trials
• Non-spherocytic hemolytic anemia due to hexokinase deficiency 0 trials
• Triosephosphate isomerase deficiency 0 trials