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Nephronophthisis 12
MONDO:0013442Any 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
1 clinical trial for this condition and its sub-types, 0 tagged with Nephronophthisis 12 itself.
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