retinoschisin 1

Preferred Label : retinoschisin 1;

Approved symbol HGNC : RS1;

Alias symbols HGNC : XLRS1;

Chromosome HGNC : Xp22.13;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000102104;

Details

Origin ID

HGNC:10457;

UMLS CUI

C1419764;

Automatic exact mappings (from CISMeF team)
- Retinoschisin [OMIM gene]
- Retinoschisis 1, X-linked, juvenile [OMIM Phenotype]
- retinoschisin 1 [ORDO Gene]
NCIt concept
- RS1 Gene [NCIt concept]
OMIM gene
- Retinoschisin [OMIM gene]
Orphanet gene
- retinoschisin 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RS1 Gene [NCIt concept]
- RS1 gene [LOINC component]
- Retinoschisin [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients