3-methylcrotonyl-CoA carboxylase 2 deficiency

Rare Disease

MONDO:0008862

Also Known As

3-Methylcrotonyl-CoA carboxylase 2 deficiency3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC2MCCC2 3-methylcrotonyl-CoA carboxylase deficiency3 alpha methylcrotonyl-CoA carboxylase 2 deficiency3 alpha methylcrotonylglycinuria 23-METHYLCROTONYL-CoA carboxylase 2 deficiency3-methylcrotonylglycinuria 2MCC 2 deficiencyMCC2 deficiencyMCC2Dmethylcrotonylglycinuria type 2methylcrotonylglycinuria, type 2

Definition

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

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Associated Genes

MCCC2 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:210210 ↗

GARD

GARD:9151 ↗

Related Diseases

3-methylcrotonyl-CoA carboxylase 1 deficiency

MONDO:0008861

Rare

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