3-methylcrotonyl-CoA carboxylase 2 deficiency

Definition

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 — per MONDO

Also identified as

• DOID 0080580 per MONDO
• MESH C535309 per MONDO
• OMIM 210210 per MONDO
• UMLS C1859499 per MONDO