Retinitis pigmentosa 36
MONDO:0012523Any retinitis pigmentosa in which the cause of the disease is a mutation in the PRCD gene.
Also known as: PRCD retinitis pigmentosa, RP36, retinitis pigmentosa 36, retinitis pigmentosa caused by mutation in PRCD, retinitis pigmentosa type 36, RP 36
25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 36 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.