Foveal hypoplasia 1

Any foveal hypoplasia in which the cause of the disease is a mutation in the PAX6 gene.

Also known as: PAX6 foveal hypoplasia, foveal hypoplasia 1, foveal hypoplasia caused by mutation in PAX6, foveal hypoplasia type 1, FVH1, O Donnell Pappas syndrome, foveal hypoplasia 1 with or without anterior segment anomalies and/or cataract, foveal hypoplasia, congenital nystagmus, corneal pannus, and presenile cataracts

2876 clinical trials for this condition and its sub-types, 0 tagged with Foveal hypoplasia 1 itself.