rhodopsin - CISMeF

Preferred Label : rhodopsin;

Approved symbol HGNC : RHO;

Name synonyms HGNC : opsin 2; rod pigment;

Alias symbols HGNC : OPN2; CSNBAD1;

Chromosome HGNC : 3q22.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000163914;

Details

Origin ID

HGNC:10012;

UMLS CUI

C1419385;

Automatic exact mappings (from CISMeF team)
- Night blindness, congenital stationary, autosomal dominant 1 [OMIM Phenotype]
- Rhodopsin [OMIM gene]
- Rhodopsin [FMA entity]
- Rhodopsin [NCIt concept]
- Rhodopsin (substance) [SNOMED CT concept]
- rhodopsin [ORDO Gene]
- rhodopsin [MeSH concept]
- rhodopsin [SNOMED Notion]
- rhodopsin [MeSH Descriptor]
NCIt concept
- RHO Gene [NCIt concept]
OMIM gene
- Rhodopsin [OMIM gene]
Orphanet gene
- rhodopsin [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RHO Gene [NCIt concept]
- Rhodopsin [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients