BBS9 - Gene browser | 3billion

BBS9

BBS9

Bardet-Biedl syndrome 9

HCNC Approved Symbol: BBS9 (HGNC:30000)
Genomic Coordinates: 7:33,129,285 - 33,635,767 (7p14.3)
Synonyms: B1, PTHB1
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the BBS9 gene.

Frequently observed phenotypes(Top 5 only)

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

02
Patient count

Obesity: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Polydactyly: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)
Retinitis pigmentosa: 2 (100.0%)
Patient Count: 2 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (100.0%)

Last updated: 2024-06-30

BBS9 - Gene browser | 3billion