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Disease Ontology Browser
Joubert syndrome 18 (DOID:0110987)
Alliance: disease page
Synonyms: JBTS18
Alt IDs: OMIM:614815
Definition: A Joubert syndrome that has_material_basis_in homozygous mutation in the TCTN3 gene on chromosome 10q24.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.13
The Jackson Laboratory