Cone-rod dystrophy 19
MONDO:0014372Any cone-rod dystrophy in which the cause of the disease is a mutation in the TTLL5 gene.
Also known as: CORD19, TTLL5 cone-rod dystrophy, cone-rod dystrophy 19, cone-rod dystrophy caused by mutation in TTLL5, cone-rod dystrophy type 19
25 clinical trials for this condition and its sub-types, 0 tagged with Cone-rod dystrophy 19 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.