3-Methylglutaconic aciduria, type I

Preferred Label : 3-Methylglutaconic aciduria, type I;

MeSH synonym : MGA, type I; 3-Methylglutaconyl-CoA hydratase deficiency; 3-Mg-CoA-Hydratase deficiency;

Details

Origin ID

C562801;

UMLS CUI

C0342727;

Automatic exact mappings (from CISMeF team)
- Methylglutaconyl-CoA Hydratase, Mitochondrial [NCIt concept]
Currated CISMeF NLP mapping
- 3 methylglutaconic aciduria type I [Disease (Nov.)]
- 3-Methylglutaconic Aciduria Type 1 [NCIt concept]
- 3-Methylglutaconic aciduria type 1 (disorder) [SNOMED CT concept]
- 3-methylglutaconic aciduria type 1 [ICD-11 More detail]
- 3-methylglutaconic aciduria type 1 [DO Concept]
- 3-methylglutaconic aciduria type 1 [ORDO Disease]
- 3-methylglutaconic aciduria, type I [OMIM Phenotype]
MeSH term(s) associated for indexing
- metabolism, inborn errors [MeSH Descriptor]
Record concept(s)
- 3-Methylglutaconic aciduria, type I [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 3 methylglutaconic aciduria type I [Disease (Nov.)]
- 3-Methylglutaconic Aciduria Type 1 [NCIt concept]
- 3-Methylglutaconic aciduria type 1 (disorder) [SNOMED CT concept]
- 3-methylglutaconic aciduria, type I [OMIM Phenotype]
Validated automatic mappings to NTBT
- 3-Methylglutaconic Aciduria [NCIt concept]

Keyword's position in hierarchy(ies) :

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