15-hydroxyprostaglandin dehydrogenase

Preferred Label : 15-hydroxyprostaglandin dehydrogenase;

Symbol : HPGD;

CISMeF acronym : HPGD;

Type : Gene;

Alternative titles and symbols : 15-hydroxyprostaglandin dehydrogenase, type I; PGDH1; PGDH;

Ensembl ID : ENSG00000164120;

Prefixed ID : *601688;

Details

Origin ID

601688;

UMLS CUI

C1415699;

Automatic exact mappings (from CISMeF team)
- 15-Hydroxyprostaglandin Dehydrogenase [NAD+] [NCIt concept]
- 15-hydroxyprostaglandin dehydrogenase [ORDO Gene]
- 15-hydroxyprostaglandin dehydrogenase [MeSH concept]
- 15-hydroxyprostaglandin dehydrogenase [HGNC gene]
- 15-hydroxyprostaglandin dehydrogenase [MeSH Supplementary Concept]
- Carbonyl Reductase [NADPH] 1 [NCIt concept]
- HPGD Gene [NCIt concept]
- HPGD wt Allele [NCIt concept]
- PHGDH wt Allele [NCIt concept]
- phosphoglycerate dehydrogenase [ORDO Gene]
HGNC gene
- 15-hydroxyprostaglandin dehydrogenase [HGNC gene]
NCIt concept(s)
- 15-Hydroxyprostaglandin Dehydrogenase [NAD+] [NCIt concept]
- HPGD Gene [NCIt concept]
- HPGD wt Allele [NCIt concept]
ORDO concept(s)
- 15-hydroxyprostaglandin dehydrogenase [ORDO Gene]
Phenotypes related
- Digital clubbing, isolated congenital [OMIM Phenotype]
- Hypertrophic osteoarthropathy, primary, autosomal recessive, 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- 15-hydroxyprostaglandin dehydrogenase [HGNC gene]
- HPGD Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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