Chloride channel, kidney, b

Preferred Label : Chloride channel, kidney, b;

Symbol : CLCNKB;

CISMeF acronym : CLCNKB;

Type : Gene;

Alternative titles and symbols : CLCKB;

Ensembl ID : ENSG00000184908;

Prefixed ID : *602023;

Details

Origin ID

602023;

UMLS CUI

C1413458;

Automatic exact mappings (from CISMeF team)
- chloride voltage-gated channel Kb [HGNC gene]
- chloride voltage-gated channel Kb [ORDO Gene]
HGNC gene
- chloride voltage-gated channel Kb [HGNC gene]
ORDO concept(s)
- chloride voltage-gated channel Kb [ORDO Gene]
Phenotypes related
- Bartter syndrome, type 3 [OMIM Phenotype]
- Bartter syndrome, type 4b, neonatal, with sensorineural deafness [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- chloride voltage-gated channel Kb [HGNC gene]

Keyword's position in hierarchy(ies) :

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