Joubert Syndrome 7, also known as jbts7, is related to nephronophthisis 1 and joubert syndrome 2, and has symptoms including ataxia An important gene associated with Joubert Syndrome 7 is RPGRIP1L (RPGRIP1 Like), and among its related pathways/superpathways are Organelle biogenesis and maintenance and Ciliopathies. Affiliated tissues include brain and kidney, and related phenotypes are ataxia and intellectual disability