Parent term(s)
carbohydrate metabolic disorder
+
Term with siblings
glucose metabolism disease +
congenital disorder of deglycosylation
+
congenital disorder of glycosylation
+
congenital lactase deficiency
congenital sucrase-isomaltase deficiency
essential fructosuria
fructose-1,6-bisphosphatase deficiency
galactosemia
+
glucosephosphate dehydrogenase deficiency
+
glycogen metabolism disorder
+
hereditary fructose intolerance syndrome
intestinal disaccharidase deficiency
lactose intolerance
multiple carboxylase deficiency
+
primary hyperoxaluria
+
pyruvate carboxylase deficiency disease
pyruvate decarboxylase deficiency
Child term(s)
diabetes mellitus
+
Fanconi-Bickel syndrome
glucose-galactose malabsorption
glucose transporter type 1 deficiency syndrome
+
hyperglycemia
+
hyperinsulinism
hypoglycemia
+
phosphoglycerate kinase 1 deficiency
prediabetes syndrome
triosephosphate isomerase deficiency
denotes an 'is-a' relationship