Retinitis pigmentosa 10
MONDO:0008379Any retinitis pigmentosa in which the cause of the disease is a mutation in the IMPDH1 gene.
Also known as: IMPDH1 retinitis pigmentosa, RP10, retinitis pigmentosa 10, retinitis pigmentosa caused by mutation in IMPDH1, retinitis pigmentosa type 10
25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 10 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.