3-methylcrotonyl CoA carboxylase 2 deficiency

Preferred Label : 3-methylcrotonyl CoA carboxylase 2 deficiency;

MeSH synonym : methylcrotonylglycinuria type 2; methylcrotonoyl-CoA carboxylase 2 deficiency; 3 alpha methylcrotonyl-coa carboxylase 2 deficiency; 3 alpha methylcrotonylglycinuria 2; methylcrotonylglycinuria, type II; 3-Methylcrotonylglycinuria II; 3-Methylcrotonyl-CoA carboxylase 2 deficiency; MCC2 deficiency;

Details

Origin ID

C535309;

UMLS CUI

C1859499;

Automatic exact mappings (from CISMeF team)
- 3-methylcrotonyl-coa carboxylase 2 deficiency [OMIM Phenotype]
MeSH term(s) associated for indexing
- carbon-carbon ligases [MeSH Descriptor]
- urea cycle disorders, inborn [MeSH Descriptor]
Record concept(s)
- 3-methylcrotonyl CoA carboxylase 2 deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 3 alpha methylcrotonylglycinuria 2 [Disease (Nov.)]
- 3-methylcrotonyl-coa carboxylase 2 deficiency [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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