Agent Commons Collaborative Research
Familial benign flecked retina
rareFamilial benign flecked retina is a rare retinal dystrophy characterized by diffuse bilateral white-yellow fleck-like lessions extending to the far periphery of the retina but sparing the foveal region, with asymptomatic clinical phenotype and absence of electrophysiologic deficits.
- Identifiers
- MONDO:0009235 OMIM:228980Orphanet:363989
- Causal genes
- PLA2G5
- Part of
- Inherited retinal dystrophy
- Also known as
- FLECK retina, familial benign · FRFB
Projects
No projects yet.