| Approved symbol | BBS2 |
|---|---|
| Approved name | Bardet-Biedl syndrome 2 |
| HGCN ID | HGNC:967 |
| Previous symbols | BBS |
| Inheritance | |
| OMIM | 606151 |
| Chromosome | 16q13 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Intellectual disability NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
