Ectonucleoside triphosphate diphosphohydrolase 1

Preferred Label : Ectonucleoside triphosphate diphosphohydrolase 1;

Symbol : ENTPD1;

CISMeF acronym : ENTPD1;

Type : Gene;

Alternative titles and symbols : Cd39 antigen; Vascular atp diphosphohydrolase; CD39; ATPDase; APYRASE;

Ensembl ID : ENSG00000138185;

Prefixed ID : *601752;

Details

Origin ID

601752;

UMLS CUI

C1414412;

Automatic exact mappings (from CISMeF team)
- Apyrase (substance) [SNOMED CT concept]
- CD39 [LOINC component]
- CD39 antigen [MeSH Supplementary Concept]
- CD39 antigen [MeSH concept]
- ENTPD1 Gene [NCIt concept]
- ENTPD1 wt Allele [NCIt concept]
- Ectonucleoside Triphosphate Diphosphohydrolase 1 [NCIt concept]
- apyrase [MeSH concept]
- apyrase [MeSH Descriptor]
- apyrase [SNOMED Notion]
- ectonucleoside triphosphate diphosphohydrolase 1 [ORDO Gene]
- ectonucleoside triphosphate diphosphohydrolase 1 [HGNC gene]
HGNC gene
- ectonucleoside triphosphate diphosphohydrolase 1 [HGNC gene]
NCIt concept(s)
- ENTPD1 Gene [NCIt concept]
- ENTPD1 wt Allele [NCIt concept]
- Ectonucleoside Triphosphate Diphosphohydrolase 1 [NCIt concept]
ORDO concept(s)
- ectonucleoside triphosphate diphosphohydrolase 1 [ORDO Gene]
Phenotypes related
- Spastic paraplegia 64, autosomal recessive [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ENTPD1 Gene [NCIt concept]
- ectonucleoside triphosphate diphosphohydrolase 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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