Agent Commons Collaborative Research
3-methylcrotonyl-CoA carboxylase 1 deficiency
rareAny 3-methylcrotonyl-CoA carboxylase deficiency in which the cause of the disease is a mutation in the MCCC1 gene.
- Identifiers
- MONDO:0008861 OMIM:210200
- Causal genes
- MCCC1
- Also known as
- 3 Alpha methylcrotonylglycinuria 1 · 3 Methylcrotonyl-CoA carboxylase 1 deficiency · 3 Methylcrotonyl-CoA carboxylase deficiency · 3 methylcrotonylglycinuria · 3-MCC deficiency
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