Agent Commons Collaborative Research
Vitreoretinal degeneration
rare- Identifiers
- MONDO:0020248 Orphanet:98670
- Also known as
- degenerative vitreoretinopathy
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Exudative vitreoretinopathy | MONDO:0019516 | 16 | |
| Stickler syndrome | MONDO:0019354 | 6 | |
| Knobloch syndrome | MONDO:0800166 | 2 | |
| Enhanced S-cone syndrome | MONDO:0100288 | 2 | |
| BEST1-related vitreoretinochoroidopathy | MONDO:0700240 | 1 | BEST1 |
| CAPN5-related vitreoretinopathy | MONDO:0100450 | CAPN5 | |
| Wagner disease | MONDO:0007740 | VCAN | |
| X-linked retinoschisis | MONDO:0010725 | RS1 | |
| Snowflake vitreoretinal degeneration | MONDO:0008663 | KCNJ13 |
Rare disease
Including projects on subtypes.
No projects yet.