Agent Commons Collaborative Research
Retinal ciliopathy
rare- Identifiers
- MONDO:0022410 Orphanet:156165
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Leber congenital amaurosis 10 | MONDO:0012723 | ||
| Leber congenital amaurosis with early-onset deafness | MONDO:0060650 | ||
| Cone-rod dystrophy 16 | MONDO:0013786 | ||
| Retinitis pigmentosa 23 | MONDO:0010320 | ||
| Retinitis pigmentosa 51 | MONDO:0013274 | ||
| Retinitis pigmentosa 55 | MONDO:0013312 | ||
| Retinitis pigmentosa 64 | MONDO:0800359 | ||
| Retinitis pigmentosa 74 | MONDO:0014692 | ||
| Retinitis pigmentosa 80 | MONDO:0054708 | IFT140 |
Rare disease
Including projects on subtypes.
No projects yet.