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Up to: Inborn carbohydrate metabolic disorder · Inborn disorder of purine or pyrimidine metabolism · Pyruvate metabolism disorder

Disorder of glycolysis

1 trial tagged with this condition →

Maturity-onset diabetes of the young 8 trials · 13 incl. sub-types Sub-types →
Pyruvate kinase deficiency of red cells 10 trials
Permanent neonatal diabetes mellitus 2 trials Sub-types →
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