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Disease Ontology Browser
Joubert syndrome 9 (DOID:0111004)
Alliance: disease page
Synonyms: JBTS9
Alt IDs: OMIM:612285, MESH:C567364
Definition: A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CC2D2A gene on chromosome 4p15.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
01/21/2020
MGI 6.14
The Jackson Laboratory