chloride voltage-gated channel 5

Preferred Label : chloride voltage-gated channel 5;

Approved symbol HGNC : CLCN5;

Name synonyms HGNC : Dent disease;

Alias symbols HGNC : ClC-5; DENTS; XLRH; CLC5; XRN; hClC-K2; hCIC-K2;

Chromosome HGNC : Xp11.23;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000171365;

Details

Origin ID

HGNC:2023;

UMLS CUI

C1413454;

Automatic exact mappings (from CISMeF team)
- Chloride channel 5 [OMIM gene]
- Dent Disease [NCIt concept]
- Dent disease [DO Concept]
- Dent disease [ORDO Disease]
- Dent disease [ICD-11 More detail]
- Dent's disease [MedDRA Preferred Term]
- Dent's disease (disorder) [SNOMED CT concept]
- Nephrolithiasis, X-linked recessive, with renal failure [OMIM Phenotype]
- chloride voltage-gated channel 5 [ORDO Gene]
- dent disease [MeSH Descriptor]
- dent disease [MeSH concept]
NCIt concept
- CLCN5 Gene [NCIt concept]
OMIM gene
- Chloride channel 5 [OMIM gene]
Orphanet gene
- chloride voltage-gated channel 5 [ORDO Gene]
See also inter- (CISMeF)
- Dent disease [OMIM phenotypic series]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CLCN5 Gene [NCIt concept]
- CLCN5 gene [LOINC component]
- Chloride channel 5 [OMIM gene]

Keyword's position in hierarchy(ies) :

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