cone-rod dystrophy 10

A cone-rod dystrophy that has_material_basis_in compound heterozygous mutation in the SEMA4A gene on chromosome 1q22.

Signs and symptoms

• Epiphora
• Spicular pigmentation of the retina
• Nyctalopia
• Progressive visual loss
• Macular degeneration
• Photophobia
• Peripheral visual field loss
• Rod-cone dystrophy
• Attenuation of retinal blood vessels

Also known as: CORD10