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Disease 3-methylcrotonyl CoA carboxylase 2 deficiency

Name 3-methylcrotonyl CoA carboxylase 2 deficiency
Synonyms 3 alpha methylcrotonyl-coa carboxylase 2 deficiency | 3 alpha methylcrotonylglycinuria 2 | 3-Methylcrotonyl-CoA Carboxylase 2 Deficiency | 3-Methylcrotonylglycinuria II | MCC2D | MCC2 Deficiency | methylcrotonoyl-CoA carboxylase 2 deficiency | Methylcrotonylglycinuria type 2 | Methylcrotonylglycinuria, Type II
Categories Genetic disease (inborn) | Metabolic disease | Nervous system disease
MeSH® ID C535309
OMIM® ID 210210

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1. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Central Nervous System Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Brain Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Brain Diseases, Metabolic Has associated chemicals Has associated genes Has associated phenotype references Brain Diseases, Metabolic, Inborn Has associated chemicals Has associated genes Has associated phenotype references Urea Cycle Disorders, Inborn Has associated chemicals Has associated genes Has associated phenotype references 3-methylcrotonyl CoA carboxylase 2 deficiency Has associated chemicals Has associated genes Has associated phenotype references
2. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Amino Acid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Urea Cycle Disorders, Inborn Has associated chemicals Has associated genes Has associated phenotype references 3-methylcrotonyl CoA carboxylase 2 deficiency Has associated chemicals Has associated genes Has associated phenotype references
3. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Brain Diseases, Metabolic, Inborn Has associated chemicals Has associated genes Has associated phenotype references Urea Cycle Disorders, Inborn Has associated chemicals Has associated genes Has associated phenotype references 3-methylcrotonyl CoA carboxylase 2 deficiency Has associated chemicals Has associated genes Has associated phenotype references
4. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Brain Diseases, Metabolic Has associated chemicals Has associated genes Has associated phenotype references Brain Diseases, Metabolic, Inborn Has associated chemicals Has associated genes Has associated phenotype references Urea Cycle Disorders, Inborn Has associated chemicals Has associated genes Has associated phenotype references 3-methylcrotonyl CoA carboxylase 2 deficiency Has associated chemicals Has associated genes Has associated phenotype references
5. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Amino Acid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Urea Cycle Disorders, Inborn Has associated chemicals Has associated genes Has associated phenotype references 3-methylcrotonyl CoA carboxylase 2 deficiency Has associated chemicals Has associated genes Has associated phenotype references
6. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Brain Diseases, Metabolic, Inborn Has associated chemicals Has associated genes Has associated phenotype references Urea Cycle Disorders, Inborn Has associated chemicals Has associated genes Has associated phenotype references 3-methylcrotonyl CoA carboxylase 2 deficiency Has associated chemicals Has associated genes Has associated phenotype references

Top ↑ Descendants

None.