Retinitis pigmentosa 20

MONDO:0013425

Any retinitis pigmentosa in which the cause of the disease is a mutation in the RPE65 gene.

Also known as: RP20, RPE65 retinitis pigmentosa, retinitis pigmentosa 20, retinitis pigmentosa caused by mutation in RPE65, retinitis pigmentosa type 20, RP 20

33 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by