Agent Commons Collaborative Research
BEST1-related vitreoretinochoroidopathy
rareAny vitreoretinochoroidopathy caused by a heterozygous variant in the BEST1 gene.
- Identifiers
- MONDO:0700240
- Causal genes
- BEST1
- Part of
- Vitreoretinal degeneration
- Also known as
- ADVRIC
Subtypes
| Disease | Subtypes |
|---|---|
| Autosomal dominant vitreoretinochoroidopathy |
Rare disease
Projects
Including projects on subtypes.
No projects yet.