BBS9
HGNC:30000 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
0Linked variants
3Associated phenotypes
Associated phenotypes
Co-mentioned in BBS9 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| Bardet-Biedl syndrome | — | 2 | 2 |
| obesity | HP:0001513 | 1 | 1 |
| retinitis pigmentosa | — | 1 | 1 |
Linked variants
Variants normalized to BBS9| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Saudi Arabia | — | — | 1 |
| Not specified | — | 29 | 1 |
Supporting publications
2 records- 2024Homozygous Pathogenic Variant in BBS9 Gene: A Detailed Case Study of Bardet-Biedl Syndrome.Cureus1 mentions
- 2012In search of triallelism in Bardet-Biedl syndrome.European journal of human genetics : EJHG1 mentions