Bardet-Biedl syndrome 9

Preferred Label : Bardet-Biedl syndrome 9;

Approved symbol HGNC : BBS9;

Name synonyms HGNC : parathyroid hormone responsive B1 gene;

Alias symbols HGNC : PTHB1; B1;

Chromosome HGNC : 7p14.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000122507;

Details

Origin ID

HGNC:30000;

UMLS CUI

C1842747;

Automatic exact mappings (from CISMeF team)
- BBS9 wt Allele [NCIt concept]
- Bardet-Biedl syndrome 9 [ORDO Gene]
- Bardet-Biedl syndrome 9 [MeSH Supplementary Concept]
- Bardet-Biedl syndrome 9 [DO Concept]
- Bardet-Biedl syndrome 9 [MeSH concept]
- Bardet-biedl syndrome 9 [OMIM Phenotype]
- Parathyroid hormone-responsive b1 gene [OMIM gene]
NCIt concept
- BBS9 Gene [NCIt concept]
OMIM gene
- Parathyroid hormone-responsive b1 gene [OMIM gene]
Orphanet gene
- Bardet-Biedl syndrome 9 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- BBS9 Gene [NCIt concept]
- Parathyroid hormone-responsive b1 gene [OMIM gene]

Keyword's position in hierarchy(ies) :

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