Sepiapterin reductase

Preferred Label : Sepiapterin reductase;

Symbol : SPR;

CISMeF acronym : SPR;

Type : Gene;

Ensembl ID : ENSG00000116096;

Prefixed ID : *182125;

Details

Origin ID

182125;

UMLS CUI

C1420371;

Automatic exact mappings (from CISMeF team)
- Sepiapterin reductase (substance) [SNOMED CT concept]
- Substance-P Receptor [NCIt concept]
- TACR1 wt Allele [NCIt concept]
- pierre robin syndrome [MeSH Descriptor]
- sepiapterin reductase [ORDO Gene]
- sepiapterin reductase [MeSH Supplementary Concept]
- sepiapterin reductase [MeSH concept]
- sepiapterin reductase [SNOMED Notion]
- sepiapterin reductase [HGNC gene]
- tachykinin receptor 1 [HGNC gene]
HGNC gene
- sepiapterin reductase [HGNC gene]
ORDO concept(s)
- sepiapterin reductase [ORDO Gene]
Phenotypes related
- Dystonia, dopa-responsive, due to sepiapterin reductase deficiency [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- sepiapterin reductase [HGNC gene]

Keyword's position in hierarchy(ies) :

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