retina and anterior neural fold homeobox 2

Preferred Label : retina and anterior neural fold homeobox 2;

Approved symbol HGNC : RAX2;

Alias symbols HGNC : MGC15631; ARMD6; CORD11;

Chromosome HGNC : 19p13.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000173976;

Details

Origin ID

HGNC:18286;

UMLS CUI

C1826771;

Automatic exact mappings (from CISMeF team)
- Macular degeneration, age-related, 6 [OMIM Phenotype]
- Retina and anterior neural fold homeobox 2 [OMIM gene]
- retina and anterior neural fold homeobox 2 [ORDO Gene]
OMIM gene
- Retina and anterior neural fold homeobox 2 [OMIM gene]
Orphanet gene
- retina and anterior neural fold homeobox 2 [ORDO Gene]
See also inter- (CISMeF)
- Cone-rod dystrophy 11 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Retina and anterior neural fold homeobox 2 [OMIM gene]

Keyword's position in hierarchy(ies) :

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