Methylmalonyl-coa mutase

Preferred Label : Methylmalonyl-coa mutase;

Symbol : MMUT;

CISMeF acronym : MMUT;

Type : Gene;

Alternative titles and symbols : Methylmalonyl-coa isomerase; MUT; MCM;

Ensembl ID : ENSG00000146085;

Prefixed ID : *609058;

Details

Origin ID

609058;

UMLS CUI

C1417504;

Automatic exact mappings (from CISMeF team)
- Megalencephaly-capillary malformation-polymicrogyria syndrome [ORDO Disease]
- Methylmalonyl-CoA mutase [MeSH concept]
- Methylmalonyl-CoA mutase [MeSH Descriptor]
- Methylmalonyl-coenzyme A mutase (substance) [SNOMED CT concept]
- Micron [NCIt concept]
- Mismatch Repair Protein [NCIt concept]
- PIK3CA wt Allele [NCIt concept]
- methylmalonyl-CoA mutase [ORDO Gene]
- methylmalonyl-CoA mutase [HGNC gene]
- methylmalonyl-coa mutase [SNOMED Notion]
False automatic mappings
- Medical Countermeasure [NCIt concept]
- Multimodal Ultrasound Tomography [NCIt concept]
HGNC gene
- methylmalonyl-CoA mutase [HGNC gene]
NCIt concept(s)
- MMUT Gene [NCIt concept]
- MMUT wt Allele [NCIt concept]
- Methylmalonyl-CoA Mutase, Mitochondrial [NCIt concept]
ORDO concept(s)
- methylmalonyl-CoA mutase [ORDO Gene]
Phenotypes related
- Methylmalonic aciduria due to methylmalonyl-coa mutase deficiency [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- methylmalonyl-CoA mutase [HGNC gene]

Keyword's position in hierarchy(ies) :

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