Cone-rod dystrophy 5

Any cone-rod dystrophy in which the cause of the disease is a mutation in the PITPNM3 gene.

Also known as: CORD5, PITPNM3 cone-rod dystrophy, cone-rod dystrophy 5, cone-rod dystrophy caused by mutation in PITPNM3, cone-rod dystrophy type 5

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