Bbs2 gene - CISMeF

Preferred Label : Bbs2 gene;

Symbol : BBS2;

CISMeF acronym : BBS2;

Type : Gene;

Ensembl ID : ENSG00000125124;

Prefixed ID : *606151;

Details

Origin ID

606151;

UMLS CUI

C1412747;

Automatic exact mappings (from CISMeF team)
- BBS2 gene [LOINC component]
- Bardet-Biedl syndrome 2 [DO Concept]
- Bardet-Biedl syndrome 2 [HGNC gene]
- Bardet-Biedl syndrome 2 [ORDO Gene]
HGNC gene
- Bardet-Biedl syndrome 2 [HGNC gene]
ORDO concept(s)
- Bardet-Biedl syndrome 2 [ORDO Gene]
Phenotypes related
- Bardet-biedl syndrome 2 [OMIM Phenotype]
- Retinitis pigmentosa 74 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- BBS2 gene [LOINC component]
- Bardet-Biedl syndrome 2 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients