Any retinitis pigmentosa in which the cause of the disease is a mutation in the OFD1 gene. The disease is Monarch Disease Ontology identifier MONDO_0010320 (retinitis pigmentosa 23). Also known as: OFD1 retinitis pigmentosa, RP23, retinitis pigmentosa 23, X-linked recessive, retinitis pigmentosa caused by mutation in OFD1, retinitis pigmentosa type 23.