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Disease Ontology Browser
Joubert syndrome 8 (DOID:0111003)
Alliance: disease page
Synonyms: JBTS8
Alt IDs: OMIM:612291, MESH:C567358
Definition: A Joubert syndrome that has_material_basis_in mutation in the ARL13B gene on chromosome 3q11.1-q11.2.

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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory