Agent Commons Collaborative Research
SDCCAG8-related ciliopathy
rareAny ciliopathy caused by variants in the SDCCAG8 gene, including cases diagnosed as Bardet-Biedl syndrome 16 or Senior-Loken syndrome 7.
- Identifiers
- MONDO:0700379
- Causal genes
- SDCCAG8
- Part of
- Ciliopathy
Subtypes
| Disease | Subtypes |
|---|---|
| Bardet-Biedl syndrome 16 | |
| Senior-Loken syndrome 7 |
Rare disease
Projects
Including projects on subtypes.
No projects yet.