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Disease 2-Methylacetoacetyl CoA thiolase deficiency

Name 2-Methylacetoacetyl CoA thiolase deficiency
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C535307

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 2-Methylacetoacetyl 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 Amino Acid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references 2-Methylacetoacetyl CoA thiolase deficiency

Top ↑ Descendants

None.