Solute carrier family 26, member 4

Preferred Label : Solute carrier family 26, member 4;

Symbol : SLC26A4;

CISMeF acronym : SLC26A4;

Type : Gene;

Alternative titles and symbols : Pds gene; PENDRIN;

Ensembl ID : ENSG00000091137;

Prefixed ID : *605646;

Details

Origin ID

605646;

UMLS CUI

C1418445;

Automatic exact mappings (from CISMeF team)
- SLC26A4 gene [LOINC component]
- solute carrier family 26 member 4 [ORDO Gene]
- solute carrier family 26 member 4 [HGNC gene]
HGNC gene
- solute carrier family 26 member 4 [HGNC gene]
NCIt concept(s)
- Pendrin [NCIt concept]
- SLC26A4 Gene [NCIt concept]
- SLC26A4 wt Allele [NCIt concept]
ORDO concept(s)
- solute carrier family 26 member 4 [ORDO Gene]
Phenotypes related
- Deafness, autosomal recessive 4, with enlarged vestibular aqueduct [OMIM Phenotype]
- Pendred syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC26A4 gene [LOINC component]
- solute carrier family 26 member 4 [HGNC gene]

Keyword's position in hierarchy(ies) :

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