3-methylcrotonyl-CoA carboxylase 2 deficiency

MONDO:0008862

Any 3-methylcrotonyl-CoA carboxylase deficiency in which the cause of the disease is a mutation in the MCCC2 gene.

Also known as: 3-Methylcrotonyl-CoA carboxylase 2 deficiency, 3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC2, MCCC2 3-methylcrotonyl-CoA carboxylase deficiency, 3 alpha methylcrotonyl-CoA carboxylase 2 deficiency, 3 alpha methylcrotonylglycinuria 2, 3-METHYLCROTONYL-CoA carboxylase 2 deficiency, 3-methylcrotonylglycinuria 2, MCC 2 deficiency

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

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