Cone-rod dystrophy 16

Any cone-rod dystrophy in which the cause of the disease is a mutation in the C8orf37 gene.

Also known as: C8orf37 cone-rod dystrophy, CORD16, cone-rod dystrophy 16, cone-rod dystrophy caused by mutation in C8orf37, cone-rod dystrophy type 16, retinal dystrophy with early macular involvement, retinitis pigmentosa 64

35 clinical trials for this condition and its sub-types.