solute carrier family 26 member 5

Preferred Label : solute carrier family 26 member 5;

Approved symbol HGNC : SLC26A5;

Name synonyms HGNC : neurosensory; 61; deafness; autosomal recessive;

Alias symbols HGNC : DFNB61; PRESTIN;

Chromosome HGNC : 7q22.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000170615;

Détails

Origin ID

HGNC:9359;

UMLS CUI

C1822756;

Automatic exact mappings (from CISMeF team)
- 61 (qualifier value) [SNOMED CT concept]
- AT 61 [MeSH Supplementary Concept]
- AT 61 [MeSH concept]
- Autosomal Recessive Inheritance [NCIt concept]
- Autosomal recessive inheritance [HPO term]
- Autosomal recessive inheritance (qualifier value) [SNOMED CT concept]
- DEAFNESS [WHO-ART Preferred Term]
- Deaf [MedDRA LLT]
- Deafness [MedDRA Preferred Term]
- Deafness [HPMULTI term]
- Deafness [NCIt concept]
- Hearing impairment [HPO term]
- Hearing loss [PASCAL descriptor]
- Sixty One [NCIt concept]
- Solute carrier family 26, member 5 [OMIM gene]
- deafness [MeSH Descriptor]
- deafness [ICPC-2 Rubric]
- deafness [MeSH concept]
- hearing disorders and deafness [MedlinePlus Topic]
- hearing problems in children [MedlinePlus Topic]
OMIM gene
- Solute carrier family 26, member 5 [OMIM gene]
Orphanet gene
- solute carrier family 26 member 5 [ORDO Gene]
See also inter- (CISMeF)
- Deafness, autosomal recessive 61 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC26A5 gene [LOINC component]
- Solute carrier family 26, member 5 [OMIM gene]

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