Nephronophthisis 12

Any nephronophthisis in which the cause of the disease is a mutation in the TTC21B gene.

Also known as: NPHP12, TTC21B nephronophthisis (disease), nephronophthisis (disease) caused by mutation in TTC21B, nephronophthisis 12, nephronophthisis type 12, Joubert syndrome 11

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