Cone-rod dystrophy 13

Any cone-rod dystrophy in which the cause of the disease is a mutation in the RPGRIP1 gene.

Also known as: CORD13, RPGRIP1 cone-rod dystrophy, cone-rod dystrophy 13, cone-rod dystrophy caused by mutation in RPGRIP1, cone-rod dystrophy type 13

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