Joubert syndrome 15

MONDO:0013763

Any Joubert syndrome in which the cause of the disease is a mutation in the CEP41 gene.

Also known as: CEP41 Joubert syndrome, JBTS15, Joubert syndrome 15, Joubert syndrome caused by mutation in CEP41, Joubert syndrome type 15, Joubert syndrome 12/15, digenic, Joubert syndrome 9/15, digenic

18 clinical trials for this condition and its sub-types, 0 tagged with Joubert syndrome 15 itself.

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↑ Joubert syndrome (2) ↑ Joubert syndrome with ocular defect (0)

Including sub-types (18) Tagged with Joubert syndrome 15 (0)

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