Joubert syndrome 2

MONDO:0011963

Any Joubert syndrome in which the cause of the disease is a mutation in the TMEM216 gene.

Also known as: CORS2, JBTS2, Joubert syndrome 2, Joubert syndrome caused by mutation in TMEM216, Joubert syndrome type 2, TMEM216 Joubert syndrome, cerebellooculorenal syndrome 2, Cerebellooculorenal syndrome 2

18 clinical trials for this condition and its sub-types, 0 tagged with Joubert syndrome 2 itself.

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

Including sub-types (18) Tagged with Joubert syndrome 2 (0)

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