Phosphomannomutase 2

Preferred Label : Phosphomannomutase 2;

Symbol : PMM2;

CISMeF acronym : PMM2;

Type : Gene;

Ensembl ID : ENSG00000140650;

Prefixed ID : *601785;

Details

Origin ID

601785;

UMLS CUI

C1418674;

Automatic exact mappings (from CISMeF team)
- PMM2 gene [LOINC component]
- Phosphomannomutase 2 [LOINC component]
- phosphomannomutase 2 [ORDO Gene]
- phosphomannomutase 2 [HGNC gene]
HGNC gene
- phosphomannomutase 2 [HGNC gene]
NCIt concept(s)
- PMM2 Gene [NCIt concept]
- PMM2 wt Allele [NCIt concept]
- Phosphomannomutase 2 [NCIt concept]
ORDO concept(s)
- phosphomannomutase 2 [ORDO Gene]
Phenotypes related
- Congenital disorder of glycosylation, type ia [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PMM2 Gene [NCIt concept]
- PMM2 gene [LOINC component]
- phosphomannomutase 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

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