Please sign in to follow a disease.
Retinitis pigmentosa 23
MONDO:0010320Any retinitis pigmentosa in which the cause of the disease is a mutation in the OFD1 gene.
Also known as: OFD1 retinitis pigmentosa, RP23, retinitis pigmentosa 23, retinitis pigmentosa 23, X-linked recessive, retinitis pigmentosa caused by mutation in OFD1, retinitis pigmentosa type 23, RP 23
35 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trials