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

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

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