Cone-rod dystrophy 2

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

Also known as: CORD2, CRD2, CRX cone-rod dystrophy, RCRD2, cone-rod dystrophy 2, cone-rod dystrophy caused by mutation in CRX, cone-rod dystrophy type 2, cone-rod retinal dystrophy-2

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