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Disease Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial

Name Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C564890

Top ↑ Ancestors

1. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Carbohydrate Metabolism, Inborn Errors Has associated chemicals Has associated genes Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial
2. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Carbohydrate Metabolism, Inborn Errors Has associated chemicals Has associated genes Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial
3. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Mitochondrial Diseases Has associated chemicals Has associated genes Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial

Top ↑ Descendants

None.