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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00181 |
3-Methylcrotonylglycinuria 3-Methylcrotonyl-CoA carboxylase deficiency |
3-Methylcrotonyl-CoA carboxylase (MCC) deficiency is an autosomal recessive disorder of leucine catabolism with a variable phenotype. | Inherited metabolic disorder |
(MCC1D) MCCC1 [HSA:56922] [KO:K01968] (MCC2D) MCCC2 [HSA:64087] [KO:K01969] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |