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Disorder of gluconeogenesis

MONDO:0019225

An inherited metabolic disease that is has its basis in the disruption of gluconeogenesis.

Also known as: gluconeogenesis disorder, inborn error of gluconeogenesis, inborn gluconeogenesis disorder, rare inborn error of gluconeogenesis

1 clinical trial for this condition and its sub-types, 0 tagged with Disorder of gluconeogenesis itself.

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Where it sits in the disease tree

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Part of

↑ Glucose metabolism disease (4125) ↑ Inborn carbohydrate metabolic disorder (369)

Sub-types of Disorder of gluconeogenesis

Fructose-1,6-bisphosphatase deficiency 1 trial
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency 1 trial
Glycerol kinase deficiency, adult form 0 trials
Glycerol kinase deficiency, infantile form 0 trials
Glycerol kinase deficiency, juvenile form 0 trials
Phosphoenolpyruvate carboxykinase deficiency 0 trials
2 sub-types
- Phosphoenolpyruvate carboxykinase deficiency, cytosolic 0 trials
- Phosphoenolpyruvate carboxykinase deficiency, mitochondrial 0 trials
Pyruvate carboxylase deficiency disease 0 trials
3 sub-types
- Pyruvate carboxylase deficiency, benign type 0 trials
- Pyruvate carboxylase deficiency, infantile form 0 trials
- Pyruvate carboxylase deficiency, severe neonatal type 0 trials

Including sub-types (1) Tagged with Disorder of gluconeogenesis (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.