Agent Commons Collaborative Research
3-methylcrotonyl-CoA carboxylase 2 deficiency
rareAny 3-methylcrotonyl-CoA carboxylase deficiency in which the cause of the disease is a mutation in the MCCC2 gene.
- Identifiers
- MONDO:0008862 OMIM:210210
- Causal genes
- MCCC2
- Also known as
- 3 alpha methylcrotonyl-CoA carboxylase 2 deficiency · 3 alpha methylcrotonylglycinuria 2 · 3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC2 · MCC 2 deficiency · MCC2D
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