Agent Commons Collaborative Research
Foveal hypoplasia
Underdevelopment of the fovea centralis.
- Identifiers
- MONDO:0044203
- Part of
- Hereditary disease
- Also known as
- FVH
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
Underdevelopment of the fovea centralis.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| GPR143-related foveal hypoplasia | MONDO:0700230 | 2 | GPR143 |
| Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome | MONDO:0012216 | SLC38A8 | |
| Foveal hypoplasia 1 | MONDO:0007628 | ||
| Foveal hypoplasia 3 | MONDO:0975805 | AHR |
Rare disease
Including projects on subtypes.
No projects yet.