Bardet-Biedl syndrome 2

Preferred Label : Bardet-Biedl syndrome 2;

Approved symbol HGNC : BBS2;

Chromosome HGNC : 16q13;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000125124;

Details

Origin ID

HGNC:967;

UMLS CUI

C1412747;

Automatic exact mappings (from CISMeF team)
- Bardet-Biedl syndrome 2 [ORDO Gene]
- Bardet-Biedl syndrome 2 [MeSH concept]
- Bardet-Biedl syndrome 2 [MeSH Supplementary Concept]
- Bardet-Biedl syndrome 2 [DO Concept]
- Bardet-biedl syndrome 2 [OMIM Phenotype]
- Bbs2 gene [OMIM gene]
OMIM gene
- Bbs2 gene [OMIM gene]
Orphanet gene
- Bardet-Biedl syndrome 2 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- BBS2 gene [LOINC component]
- Bbs2 gene [OMIM gene]

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