retinitis pigmentosa GTPase regulator

Preferred Label : retinitis pigmentosa GTPase regulator;

Approved symbol HGNC : RPGR;

Alias symbols HGNC : CORDX1;

Chromosome HGNC : Xp11.4;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000156313;

Details

Origin ID

HGNC:10295;

UMLS CUI

C1419623;

Automatic exact mappings (from CISMeF team)
- Cone-rod dystrophy, X-linked, 1 [OMIM Phenotype]
- Retinitis pigmentosa gtpase regulator [OMIM gene]
- retinitis pigmentosa GTPase regulator [ORDO Gene]
OMIM gene
- Retinitis pigmentosa gtpase regulator [OMIM gene]
Orphanet gene
- retinitis pigmentosa GTPase regulator [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- RPGR gene [LOINC component]
- Retinitis pigmentosa gtpase regulator [OMIM gene]

Keyword's position in hierarchy(ies) :

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