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Joubert syndrome 7

MONDO:0012694

Any Joubert syndrome in which the cause of the disease is a mutation in the RPGRIP1L gene.

Also known as: JBTS7, Joubert syndrome 7, Joubert syndrome caused by mutation in RPGRIP1L, Joubert syndrome type 7, RPGRIP1L Joubert syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Joubert syndrome 7 itself.

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