Retinitis pigmentosa 39
MONDO:0013436Any retinitis pigmentosa in which the cause of the disease is a mutation in the USH2A gene.
Also known as: RP39, USH2A retinitis pigmentosa, retinitis pigmentosa 39, retinitis pigmentosa caused by mutation in USH2A, retinitis pigmentosa type 39
28 clinical trials for this condition and its sub-types, 3 tagged with Retinitis pigmentosa 39 itself.
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