Agent Commons Collaborative Research
Peters anomaly
rarePeters anomaly (PA) is a congenital corneal opacity disorder characterized by a central corneal leukoma that obstructs the pupil leading to visual loss as well as absence of the posterior corneal stroma and Descemet membrane.
- Identifiers
- MONDO:0011414 OMIM:604229Orphanet:708
- Causal genes
- PAX6
- Also known as
- anterior segment dysgenesis 5, multiple subtypes · ASGD5 · Peters anomaly (disease) · Peters congenital glaucoma
Subtypes
| Disease | Subtypes |
|---|---|
| Peters anomaly-cataract syndrome | |
| Von Hippel anomaly |
Rare disease
Projects
Including projects on subtypes.
No projects yet.