inborn carbohydrate metabolic disorder
MONDO:0019214Mondo
Findings
No curated finding names inborn carbohydrate metabolic disorder yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An inherited metabolic disease that is has its basis in the disruption of carbohydrate metabolic process.
Definition from the Mondo Disease Ontology (MONDO:0019214), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (18)
- congenital disorder of deglycosylation 1
- disorder of carbohydrate transmembrane transport and absorption
- disorder of fructose metabolism
- disorder of galactose and fructose metabolism
- disorder of galactose metabolism
- disorder of gluconeogenesis
- disorder of glycogen metabolism
- disorder of glycolysis
- disorders of pentose/polyol metabolism
- G6PD deficiency
- GLUT1 deficiency syndrome
- hyperinsulinemic hypoglycemia
- lactose intolerance
- mucopolysaccharidosis
- multiple carboxylase deficiency
- oligosaccharidosis
- primary hyperoxaluria
- pyruvate dehydrogenase deficiency
Other names
4 names
Resolves to: inborn carbohydrate metabolic disorder
- Also called
- carbohydrate metabolism disorderinborn carbohydrate metabolic process disorderinborn error of carbohydrate metabolic processrare inborn error of carbohydrate metabolic process