solute carrier family 26 member 4

Preferred Label : solute carrier family 26 member 4;

Approved symbol HGNC : SLC26A4;

Name synonyms HGNC : Pendred syndrome; pendrin;

Alias symbols HGNC : PDS;

Chromosome HGNC : 7q22.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000091137;

Details

Origin ID

HGNC:8818;

UMLS CUI

C1418445;

Automatic exact mappings (from CISMeF team)
- Pendred Syndrome [NCIt concept]
- Pendred syndrome [OMIM Phenotype]
- Pendred syndrome [ORDO Disease]
- Solute carrier family 26, member 4 [OMIM gene]
- solute carrier family 26 member 4 [ORDO Gene]
NCIt concept
- SLC26A4 Gene [NCIt concept]
OMIM gene
- Solute carrier family 26, member 4 [OMIM gene]
Orphanet gene
- solute carrier family 26 member 4 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC26A4 gene [LOINC component]
- Solute carrier family 26, member 4 [OMIM gene]

Keyword's position in hierarchy(ies) :

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