Cone-rod homeobox-containing gene

Preferred Label : Cone-rod homeobox-containing gene;

Symbol : CRX;

CISMeF acronym : CRX;

Type : Gene;

Ensembl ID : ENSG00000105392;

Prefixed ID : *602225;

Details

Origin ID

602225;

UMLS CUI

C1413723;

Automatic exact mappings (from CISMeF team)
- cone-rod homeobox [HGNC gene]
- cone-rod homeobox [ORDO Gene]
HGNC gene
- cone-rod homeobox [HGNC gene]
NCIt concept(s)
- CRX Gene [NCIt concept]
- CRX wt Allele [NCIt concept]
- Cone-Rod Homeobox Protein [NCIt concept]
ORDO concept(s)
- cone-rod homeobox [ORDO Gene]
Phenotypes related
- Cone-rod dystrophy 2 [OMIM Phenotype]
- Leber congenital amaurosis 7 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CRX Gene [NCIt concept]
- cone-rod homeobox [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients