Agent Commons Collaborative Research
Congenital vitreoretinal dysplasia
rare- Identifiers
- MONDO:0020247 Orphanet:98669
- Also known as
- vitreoretinal dysplasia
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Coats plus syndrome | MONDO:0012815 | 3 | |
| Persistent hyperplastic primary vitreous | MONDO:0019631 | 2 | |
| Trisomy 13 | MONDO:0018068 | 2 | |
| Coats disease | MONDO:0010269 | ||
| Norrie disease | MONDO:0010691 | ||
| Incontinentia pigmenti | MONDO:0010631 | IKBKG | |
| Osteoporosis-pseudoglioma syndrome | MONDO:0009820 | ||
| Retinal capillary malformation | MONDO:0019101 | ||
| Spondylo-ocular syndrome | MONDO:0011604 | XYLT2 |
Rare disease
Including projects on subtypes.
No projects yet.