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Disease Ontology Browser
Joubert syndrome 7 (DOID:0111002)
Alliance: disease page
Synonyms: JBTS7
Alt IDs: OMIM:611560, MESH:C566916
Definition: A Joubert syndrome that has_material_basis_in mutation in the RPGRIP1L gene on chromosome 16q12.2.

Disease References using Mouse Models (1)

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
11/12/2019
MGI 6.14
The Jackson Laboratory