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Cone-rod dystrophy 5

MONDO:0010969

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

25 clinical trials for this condition and its sub-types, 0 tagged with Cone-rod dystrophy 5 itself.

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