GUCY2D retinopathy
MONDO:0100454Any inherited retinal dystrophy in which the cause of the disease is a mutation in the GUCY2D gene.
Also known as: retinopathy caused by mutation in GUCY2D
26 clinical trials for this condition and its sub-types, 0 tagged with GUCY2D retinopathy itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of GUCY2D retinopathy
-
Cone-rod dystrophy 6 1 trial
-
GUCY2D-related recessive retinopathy 0 trials · 1 incl. sub-types
2 sub-types
-
GUCY2D-related dominant retinopathy 0 trials
1 sub-type
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.