disorder of glycolysis
MONDO:0017688Mondo
Findings
No curated finding names disorder of glycolysis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Where it sits
- A kind of
- Narrower terms (16)
- Charcot-Marie-Tooth disease type 4G
- glycogen storage disease due to aldolase A deficiency
- glycogen storage disease due to lactate dehydrogenase H-subunit deficiency
- glycogen storage disease due to lactate dehydrogenase M-subunit deficiency
- glycogen storage disease due to muscle beta-enolase deficiency
- glycogen storage disease due to phosphoglycerate kinase 1 deficiency
- glycogen storage disease due to phosphoglycerate mutase deficiency
- glycogen storage disease VII
- hemolytic anemia due to glucophosphate isomerase deficiency
- hyperinsulinemic hypoglycemia, familial, 3
- lactic aciduria due to D-lactic acid
- maturity-onset diabetes of the young
- non-spherocytic hemolytic anemia due to hexokinase deficiency
- permanent neonatal diabetes mellitus
- pyruvate kinase deficiency of red cells
- triosephosphate isomerase deficiency