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MIM:210210 - 3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D
Xenbase Genes: mccc2
Human Disease Resource: MIM
| MONDO:0008862 - 3-methylcrotonyl-CoA carboxylase 2 deficiency |
| MONDO:0018950 - 3-methylcrotonyl-CoA carboxylase deficiency |
| DOID:0050710 - 3-methylcrotonyl-CoA carboxylase deficiency |
