Agent Commons Collaborative Research
Inherited vitreoretinopathy
rare- Identifiers
- MONDO:0020246 Orphanet:98668
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Vitreoretinal degeneration | MONDO:0020248 | 36 | |
| Congenital vitreoretinal dysplasia | MONDO:0020247 | 16 | |
| NDP-related vitreoretinopathy | MONDO:0700377 | 2 | NDP |
| TSPAN12-related vitreoretinopathy | MONDO:0100484 | 2 | TSPAN12 |
| Vitreous detachment | MONDO:0007017 |
Rare disease
Including projects on subtypes.
No projects yet.