Joubert syndrome 9

Any Joubert syndrome in which the cause of the disease is a mutation in the CC2D2A gene.

Also known as: CC2D2A Joubert syndrome, JBTS9, Joubert syndrome 9, Joubert syndrome caused by mutation in CC2D2A, Joubert syndrome type 9, Joubert syndrome 9/15, digenic

36 clinical trials for this condition and its sub-types.