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Summary Literature (0)
MIM:614970 - JOUBERT SYNDROME 20; JBTS20

Xenbase Genes: tmem231

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013994 - Joubert syndrome 20
MONDO:0016364 - Joubert syndrome with ocular defect
MONDO:0018772 - Joubert syndrome

Disease Ontology (DO):
DOID:0110989 - Joubert syndrome 20