Joubert Syndrome 9 (JBTS9)

Joubert Syndrome 9, also known as jbts9, is related to joubert syndrome 1 and ocular motor apraxia. An important gene associated with Joubert Syndrome 9 is CC2D2A (Coiled-Coil And C2 Domain Containing 2A). Affiliated tissues include kidney and brain, and related phenotypes are intellectual disability and global developmental delay