usherin - CISMeF

Preferred Label : usherin;

Approved symbol HGNC : USH2A;

Alias symbols HGNC : RP39;

Chromosome HGNC : 1q41;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000042781;

Details

Origin ID

HGNC:12601;

UMLS CUI

C1421381;

Automatic exact mappings (from CISMeF team)
- Retinitis pigmentosa 39 [OMIM Phenotype]
- Usher syndrome, type iia [OMIM Phenotype]
- Usherin [OMIM gene]
- usherin [ORDO Gene]
OMIM gene
- Usherin [OMIM gene]
Orphanet gene
- usherin [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- USH2A gene [LOINC component]
- Usherin [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