Any cone-rod dystrophy in which the cause of the disease is a mutation in the RPGRIP1 gene. The disease is Monarch Disease Ontology id MONDO_0011987 (cone-rod dystrophy 13). Also known as: CORD13, RPGRIP1 cone-rod dystrophy, cone-rod dystrophy caused by mutation in RPGRIP1, cone-rod dystrophy type 13.