3-methylcrotonyl-CoA carboxylase 1 deficiency

Any 3-methylcrotonyl-CoA carboxylase deficiency in which the cause of the disease is a mutation in the MCCC1 gene.

Also known as: 3-Methylcrotonyl-Coa carboxylase 1 deficiency, 3-methylcrotonyl-CoA carboxylase 1 deficiency, 3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC1, MCCC1 3-methylcrotonyl-CoA carboxylase deficiency, 3 Alpha methylcrotonylglycinuria 1, 3 Methylcrotonyl-CoA carboxylase 1 deficiency, 3 Methylcrotonyl-CoA carboxylase deficiency, 3 alpha methylcrotonylglycinuria 1

5 clinical trials for this condition and its sub-types.