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Summary Literature (0)
MIM:611560 - JOUBERT SYNDROME 7; JBTS7

Xenbase Genes: rpgrip1l

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012308 - Joubert syndrome with renal defect
MONDO:0012694 - Joubert syndrome 7

Disease Ontology (DO):
DOID:0111002 - Joubert syndrome 7