cone-rod dystrophy 15

A cone-rod dystrophy that has_material_basis_in homozygous mutation in the CDHR1 gene on chromosome 10q23.

Signs and symptoms

• Progressive visual loss
• Constriction of peripheral visual field
• Color vision defect
• Rod-cone dystrophy
• Retinal pigment epithelial atrophy
• Attenuation of retinal blood vessels
• Nyctalopia
• Photophobia

Also known as: CORD15