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Metadata
ID	DOID:0111004
Name	Joubert syndrome 9
Definition	A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CC2D2A gene on chromosome 4p15. https://www.ncbi.nlm.nih.gov/pubmed/18387594
Xrefs	MESH:C567364 OMIM:612285
Synonyms	JBTS9 [EXACT]
Parent Relationships	is_a digenic disease is_a Joubert syndrome