3-Methylcrotonyl-CoA carboxylase deficiency

Preferred Label : 3-Methylcrotonyl-CoA carboxylase deficiency;

LOINC status : ACTIVE;

Origin ID

LP174560-5;

UMLS CUI

C4551505;

Automatic exact mappings (from CISMeF team)
- 3-Methylcrotonyl-CoA carboxylase deficiency [DO Concept]
- 3-methylcrotonyl CoA carboxylase 1 deficiency [MeSH Supplementary Concept]
- 3-methylcrotonyl-CoA carboxylase deficiency [ORDO Disease]
- Methylcrotonyl-CoA Carboxylase Deficiency [NCIt concept]
- Methylcrotonyl-coenzyme A carboxylase deficiency (disorder) [SNOMED CT concept]
LOINC code(s)
- 3-Methylcrotonyl-CoA carboxylase deficiency:Imp:Pt:Bld.dot:Nom: [LOINC code]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Methylcrotonyl-CoA Carboxylase Deficiency [NCIt concept]
- Methylcrotonyl-coenzyme A carboxylase deficiency (disorder) [SNOMED CT concept]