bisphosphoglycerate mutase

Preferred Label : bisphosphoglycerate mutase;

Approved symbol HGNC : BPGM;

Chromosome HGNC : 7q33;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000172331;

Details

Origin ID

HGNC:1093;

UMLS CUI

C1412816;

Automatic exact mappings (from CISMeF team)
- Bisphosphoglycerate Mutase [NCIt concept]
- Bisphosphoglycerate mutase [LOINC component]
- Bisphosphoglycerate mutase (substance) [SNOMED CT concept]
- bisphosphoglycerate mutase [ORDO Gene]
- bisphosphoglycerate mutase [MeSH Descriptor]
- bisphosphoglycerate mutase [SNOMED Notion]
- bisphosphoglycerate mutase [MeSH concept]
Currated CISMeF NLP mapping
- BPGM Gene [NCIt concept]
- BPGM gene [LOINC component]
- Bisphosphoglycerate mutase [OMIM gene]
NCIt concept
- BPGM Gene [NCIt concept]
OMIM gene
- Bisphosphoglycerate mutase [OMIM gene]
Orphanet gene
- bisphosphoglycerate mutase [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- BPGM Gene [NCIt concept]
- BPGM gene [LOINC component]
- Bisphosphoglycerate mutase [OMIM gene]
- Hemolytic anemia due to diphosphoglycerate mutase deficiency [ORDO Disease]

Keyword's position in hierarchy(ies) :

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