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Disease Ontology Browser
Joubert syndrome 10 (DOID:0110981)
Alliance: disease page
Synonyms: JBTS10
Alt IDs: OMIM:300804, MESH:C567582
Definition: A Joubert syndrome that has_material_basis_in X-linked recessive inheritance of mutation in the OFD1 gene on chromosome Xp22.2.

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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last database update
MGI 6.13
The Jackson Laboratory