Cone-rod dystrophy 21

MONDO:0014669

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

25 clinical trials for this condition and its sub-types, 0 tagged with Cone-rod dystrophy 21 itself.

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↑ Cone-rod dystrophy (21)

Including sub-types (25) Tagged with Cone-rod dystrophy 21 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.