/3-methylcrotonyl-CoA carboxylase 1 deficiency

3-methylcrotonyl-CoA carboxylase 1 deficiency

Rare Disease

MONDO:0008861

Also Known As

3-Methylcrotonyl-Coa carboxylase 1 deficiency3-methylcrotonyl-CoA carboxylase 1 deficiency3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC1MCCC1 3-methylcrotonyl-CoA carboxylase deficiency3 Alpha methylcrotonylglycinuria 13 Methylcrotonyl-CoA carboxylase 1 deficiency3 Methylcrotonyl-CoA carboxylase deficiency3 alpha methylcrotonylglycinuria 13 methylcrotonylglycinuria3-MCC deficiency3-METHYLCROTONYL-CoA carboxylase 1 deficiency3-Methylcrotonyl-Coa carboxylase deficiency3-Methylcrotonyl-Coenzyme A carboxylase deficiency3-methylcrotonylglycinuria3-methylcrotonylglycinuria 13-methylcrotonylglycinuria IBmcc deficiencyMCC 1 deficiencyMCC deficiencyMCC1 deficiencyMCC1DMCCD type 1Mcc1 deficiencyMccd type 1Methylcrotonyl-Coa carboxylase deficiencydeficiency of methylcrotonoyl-Coa carboxylasemethylcrotonoyl-CoA carboxylase 1 deficiencymethylcrotonylglycinuria type 1methylcrotonylglycinuria type I