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Joubert syndrome 9

MONDO:0012849

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

18 clinical trials for this condition and its sub-types, 0 tagged with Joubert syndrome 9 itself.

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Part of

↑ Joubert syndrome (2) ↑ Joubert syndrome with oculorenal defect (1)

Including sub-types (18) Tagged with Joubert syndrome 9 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.