Bardet-Biedl syndrome 7

Preferred Label : Bardet-Biedl syndrome 7;

Approved symbol HGNC : BBS7;

Alias symbols HGNC : FLJ10715; BBS2L1;

Chromosome HGNC : 4q27;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000138686;

Details

Origin ID

HGNC:18758;

UMLS CUI

C1425764;

Automatic exact mappings (from CISMeF team)
- Bardet-Biedl syndrome 7 [ORDO Gene]
- Bardet-Biedl syndrome 7 [DO Concept]
- Bardet-Biedl syndrome 7 [MeSH Supplementary Concept]
- Bardet-Biedl syndrome 7 [MeSH concept]
- Bardet-biedl syndrome 7 [OMIM Phenotype]
- Bbs7 gene [OMIM gene]
OMIM gene
- Bbs7 gene [OMIM gene]
Orphanet gene
- Bardet-Biedl syndrome 7 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Bbs7 gene [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients