Cone-rod dystrophy 20

Any cone-rod dystrophy in which the cause of the disease is a mutation in the POC1B gene.

Also known as: CORD20, POC1B cone-rod dystrophy, cone-rod dystrophy 20, cone-rod dystrophy caused by mutation in POC1B, cone-rod dystrophy type 20

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