Renin - CISMeF

Preferred Label : Renin;

Symbol : REN;

CISMeF acronym : REN;

Type : Gene;

Ensembl ID : ENSG00000143839;

Prefixed ID : *179820;

Details

Origin ID

179820;

UMLS CUI

C1419338;

Automatic exact mappings (from CISMeF team)
- Kidney [LOINC System]
- REN Gene [NCIt concept]
- Renin [NCIt concept]
- Renin [LOINC component]
- Renin [MedDRA Preferred Term]
- Renin (substance) [SNOMED CT concept]
- Renin Measurement [NCIt concept]
- potassium channel tetramerization domain containing 11 [HGNC gene]
- renin [ORDO Gene]
- renin [SNOMED Notion]
- renin [HGNC gene]
- renin [MeSH Descriptor]
- renin [MeSH concept]
HGNC gene
- renin [HGNC gene]
NCIt concept(s)
- REN Gene [NCIt concept]
- REN wt Allele [NCIt concept]
- Renin [NCIt concept]
ORDO concept(s)
- renin [ORDO Gene]
Phenotypes related
- Renal tubular dysgenesis [OMIM Phenotype]
- Tubulointerstitial kidney disease, autosomal dominant, 4 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- REN Gene [NCIt concept]
- renin [HGNC gene]

Keyword's position in hierarchy(ies) :

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