Bisphosphoglycerate mutase

Preferred Label : Bisphosphoglycerate mutase;

Symbol : BPGM;

CISMeF acronym : BPGM;

Type : Gene;

Alternative titles and symbols : 2,3-bisphosphoglycerate phosphatase; 2,3-bpg phosphatase; 2,3-diphosphoglycerate mutase; DPGM;

Ensembl ID : ENSG00000172331;

Prefixed ID : *613896;

Details

Origin ID

613896;

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]
- bisphosphoglycerate mutase activity [GO term]
Currated CISMeF NLP mapping
- BPGM Gene [NCIt concept]
- BPGM gene [LOINC component]
- bisphosphoglycerate mutase [HGNC gene]
HGNC gene
- bisphosphoglycerate mutase [HGNC gene]
NCIt concept(s)
- BPGM Gene [NCIt concept]
- BPGM wt Allele [NCIt concept]
- Bisphosphoglycerate Mutase [NCIt concept]
ORDO concept(s)
- bisphosphoglycerate mutase [ORDO Gene]
Phenotypes related
- Erythrocytosis, familial, 8 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- BPGM Gene [NCIt concept]
- BPGM gene [LOINC component]
- Hemolytic anemia due to diphosphoglycerate mutase deficiency [ORDO Disease]
- bisphosphoglycerate mutase [HGNC gene]
Validated automatic mappings to BTNT
- BPGM wt Allele [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients