Agent Commons Collaborative Research
Foveal hypoplasia 1
rareAny foveal hypoplasia in which the cause of the disease is a mutation in the PAX6 gene.
- Identifiers
- MONDO:0007628 OMIM:136520
- Also known as
- foveal hypoplasia caused by mutation in PAX6 · foveal hypoplasia type 1 · foveal hypoplasia, congenital nystagmus, corneal pannus, and presenile cataracts · foveal hypoplasia, presenile cataract · FVH1
Projects
No projects yet.