Barttin clcnk-type accessory subunit beta

Preferred Label : Barttin clcnk-type accessory subunit beta;

Symbol : BSND;

CISMeF acronym : BSND;

Type : Gene;

Alternative titles and symbols : BARTTIN; Bsnd gene;

Ensembl ID : ENSG00000162399;

Prefixed ID : *606412;

Details

Origin ID

606412;

UMLS CUI

C1424344;

Automatic exact mappings (from CISMeF team)
- BSND Gene [NCIt concept]
- Bartter disease type 4a [DO Concept]
- Barttin [NCIt concept]
- barttin CLCNK type accessory subunit beta [HGNC gene]
- barttin CLCNK type accessory subunit beta [ORDO Gene]
HGNC gene
- barttin CLCNK type accessory subunit beta [HGNC gene]
NCIt concept(s)
- BSND Gene [NCIt concept]
- BSND wt Allele [NCIt concept]
- Barttin [NCIt concept]
ORDO concept(s)
- barttin CLCNK type accessory subunit beta [ORDO Gene]
Phenotypes related
- Bartter syndrome, type 4a, neonatal, with sensorineural deafness [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- BSND Gene [NCIt concept]
- barttin CLCNK type accessory subunit beta [HGNC gene]

Keyword's position in hierarchy(ies) :

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