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Disease Methylmalonyl-CoA Epimerase Deficiency with Sepiapterin Reductase Deficiency

Name Methylmalonyl-CoA Epimerase Deficiency with Sepiapterin Reductase Deficiency
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C565387

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 Amino Acid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Methylmalonyl-CoA Epimerase Deficiency with Sepiapterin Reductase Deficiency
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 Amino Acid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Methylmalonyl-CoA Epimerase Deficiency with Sepiapterin Reductase Deficiency

Top ↑ Descendants

None.