Ectonucleotide pyrophosphatase/phosphodiesterase 1

Preferred Label : Ectonucleotide pyrophosphatase/phosphodiesterase 1;

Symbol : ENPP1;

CISMeF acronym : ENPP1;

Type : Gene;

Alternative titles and symbols : Alkaline phosphodiesterase I; Plasma cell membrane glycoprotein pc-1; Membrane component, chromosome 6, surface marker 1; Ly41, mouse, homolog of; Phosphodiesterase I/nucleotide pyrophosphatase 1; Nucleotide pyrophosphatase; PDNP1; PC1; PCA1; M6S1; NPPS;

Ensembl ID : ENSG00000197594;

Prefixed ID : *173335;

Details

Origin ID

173335;

UMLS CUI

C1414407;

Automatic exact mappings (from CISMeF team)
- ENPP1 wt Allele [NCIt concept]
- Ectonucleotide Pyrophosphatase/Phosphodiesterase Family Member 1 [NCIt concept]
- KRT16 wt Allele [NCIt concept]
- N-(3-pyridyl)-3-phenylsuccinimide [MeSH Supplementary Concept]
- Neuroendocrine Convertase 1 [NCIt concept]
- Nucleotide pyrophosphatase (substance) [SNOMED CT concept]
- PC1 (body structure) [SNOMED CT concept]
- PCA-1 [LOINC component]
- PCAT1 wt Allele [NCIt concept]
- PCSK1 wt Allele [NCIt concept]
- Proprotein convertase 1 (substance) [SNOMED CT concept]
- Prostate Cancer Associated Transcript 1 [NCIt concept]
- ectonucleotide pyrophosphatase phosphodiesterase 1 [MeSH Supplementary Concept]
- ectonucleotide pyrophosphatase phosphodiesterase 1 [MeSH concept]
- ectonucleotide pyrophosphatase/phosphodiesterase 1 [ORDO Gene]
- nucleotide pyrophosphatase [SNOMED Notion]
- nucleotide pyrophosphatase [MeSH concept]
- nucleotide pyrophosphatase [MeSH Supplementary Concept]
- phosphodiesterase i [MeSH Descriptor]
- proprotein convertase subtilisin/kexin type 1 [ORDO Gene]
Currated CISMeF NLP mapping
- ENPP1 Gene [NCIt concept]
- ectonucleotide pyrophosphatase/phosphodiesterase 1 [HGNC gene]
HGNC gene
- ectonucleotide pyrophosphatase/phosphodiesterase 1 [HGNC gene]
NCIt concept(s)
- ENPP1 Gene [NCIt concept]
- ENPP1 wt Allele [NCIt concept]
- Ectonucleotide Pyrophosphatase/Phosphodiesterase Family Member 1 [NCIt concept]
ORDO concept(s)
- ectonucleotide pyrophosphatase/phosphodiesterase 1 [ORDO Gene]
Phenotypes related
- Arterial calcification, generalized, of infancy, 1 [OMIM Phenotype]
- Cole disease [OMIM Phenotype]
- Hypophosphatemic rickets, autosomal recessive, 2 [OMIM Phenotype]
- Obesity [OMIM Phenotype]
- Type 2 diabetes mellitus [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ENPP1 Gene [NCIt concept]
- ectonucleotide pyrophosphatase/phosphodiesterase 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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