Retinitis Pigmentosa 69, also known as rp69, is related to bardet-biedl syndrome 16 and joubert syndrome 5. An important gene associated with Retinitis Pigmentosa 69 is KIZ (Kizuna Centrosomal Protein), and among its related pathways/superpathways are Ciliopathies and Joubert syndrome. Affiliated tissues include retina and eye, and related phenotypes are nyctalopia and rod-cone dystrophy