Human genes for Leber congenital amaurosis 6
Leber congenital amaurosis 6 [DOID:0110329]
A Leber congenital amaurosis that is characterized by early photophobia, hypermetropia less than +7 diopters, and visual acuity in the range of 20/400 to count fingers and has_material_basis_in mutation in the RPGRIP1 gene on chromosome 14q11.
Synonyms: Leber congenital amaurosis 6, DOID:0110329, LCA6