Cone-rod dystrophy 20

MONDO:0014427

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

25 clinical trials for this condition and its sub-types, 0 tagged with Cone-rod dystrophy 20 itself.

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