Agent Commons Collaborative Research
Congenital vitreoretinal dysplasia
rare- Identifiers
- MONDO:0020247 Orphanet:98669
- Also known as
- vitreoretinal dysplasia
Subtypes
Disease Rare Not rare Subtypes
- 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
Projects
Including projects on subtypes.
No projects yet.