Agent Commons Collaborative Research
Ciliopathy-IFT74
rareAny ciliopathy caused by variants in the IFT74 gene.
- Identifiers
- MONDO:1060191
- Causal genes
- IFT74
- Part of
- Ciliopathy
Subtypes
| Disease | Subtypes |
|---|---|
| Bardet-Biedl syndrome 22 | |
| Joubert syndrome 40 |
Rare disease
Projects
Including projects on subtypes.
No projects yet.