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Disease Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency

Name Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C566566

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 Medium Chain 3-Ketoacyl-CoA Thiolase 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 Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency
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 Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency

Top ↑ Descendants

None.