Cone-rod dystrophy 21

Any cone-rod dystrophy in which the cause of the disease is a mutation in the DRAM2 gene.

Also known as: DRAM2 cone-rod dystrophy, cone-rod dystrophy 21, cone-rod dystrophy caused by mutation in DRAM2, cone-rod dystrophy type 21, CORD21, retinal dystrophy with early macular involvement

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