Cone-rod dystrophy 15

MONDO:0013348

Any cone-rod dystrophy in which the cause of the disease is a mutation in the CDHR1 gene.

Also known as: CDHR1 cone-rod dystrophy, CORD15, cone-rod dystrophy 15, cone-rod dystrophy caused by mutation in CDHR1, cone-rod dystrophy type 15, retinitis pigmentosa 65

25 clinical trials for this condition and its sub-types, 0 tagged with Cone-rod dystrophy 15 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Retinitis pigmentosa (89) ↑ Cone-rod dystrophy (21) ↑ CDHR1-related retinopathy (0)

Including sub-types (25) Tagged with Cone-rod dystrophy 15 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.