MeSH Browser

MeSH Supplementary: 3-methylcrotonyl CoA carboxylase 2 deficiency
Unique ID: C535309
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535309
Entry Term(s): 3 alpha methylcrotonyl-coa carboxylase 2 deficiency; 3 alpha methylcrotonylglycinuria 2; 3-Methylcrotonyl-CoA Carboxylase 2 Deficiency; 3-Methylcrotonylglycinuria II; MCC2 Deficiency; Methylcrotonylglycinuria type 2; Methylcrotonylglycinuria, Type II; methylcrotonoyl-CoA carboxylase 2 deficiency
Registry Numbers: 0
Heading Mapped to: Carbon-Carbon Ligases / deficiency; *Urea Cycle Disorders, Inborn
Frequency: 3
Date of Entry: 2010/06/25
Revision Date: 2013/11/06

3-methylcrotonyl CoA carboxylase 2 deficiency MeSH Supplementary Concept Data 2025