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Up to: Inborn errors of metabolism · Carbohydrate metabolism disease
Inborn carbohydrate metabolic disorder
An inherited metabolic disease that is has its basis in the disruption of carbohydrate metabolic process.
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Disorder of carbohydrate transmembrane transport and absorption 0 trials · 162 incl. sub-types Sub-types →
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Disorder of glycogen metabolism 15 trials · 69 incl. sub-types Sub-types →
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Mucopolysaccharidosis 14 trials · 62 incl. sub-types Sub-types →
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Disorder of glycolysis 1 trial · 27 incl. sub-types Sub-types →
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Primary hyperoxaluria 13 trials · 17 incl. sub-types Sub-types →
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Hyperinsulinemic hypoglycemia 2 trials · 14 incl. sub-types Sub-types →
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Oligosaccharidosis 0 trials · 11 incl. sub-types Sub-types →
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Lactose intolerance 9 trials · 10 incl. sub-types Sub-types →
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G6PD deficiency 6 trials Sub-types →
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GLUT1 deficiency syndrome 4 trials · 5 incl. sub-types Sub-types →
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Disorder of galactose metabolism 0 trials · 5 incl. sub-types Sub-types →
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Pyruvate dehydrogenase deficiency 2 trials · 4 incl. sub-types Sub-types →
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Disorder of galactose and fructose metabolism 0 trials · 4 incl. sub-types Sub-types →
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Multiple carboxylase deficiency 0 trials · 3 incl. sub-types Sub-types →
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Disorder of fructose metabolism 0 trials · 1 incl. sub-types Sub-types →
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Disorder of gluconeogenesis 0 trials · 1 incl. sub-types Sub-types →
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Disorders of pentose/polyol metabolism 0 trials · 1 incl. sub-types Sub-types →