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Disease Isobutyryl-CoA dehydrogenase deficiency

Name Isobutyryl-CoA dehydrogenase deficiency
Synonyms ACAD8 DEFICIENCY | Acyl-CoA dehydrogenase family, member 8, deficiency of | IBD DEFICIENCY | Isobutyryl-Coenzyme A Dehydrogenase Deficiency
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C535541
OMIM® ID 611283

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 Isobutyryl-CoA dehydrogenase deficiency Has associated chemicals Has associated genes
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 Isobutyryl-CoA dehydrogenase deficiency Has associated chemicals Has associated genes

Top ↑ Descendants

None.