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Summary Literature (0)
MIM:614464 - JOUBERT SYNDROME 15; JBTS15

Xenbase Genes: cep41

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013763 - Joubert syndrome 15
MONDO:0016364 - Joubert syndrome with ocular defect
MONDO:0018772 - Joubert syndrome

Disease Ontology (DO):
DOID:0110984 - Joubert syndrome 15