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Disease Ontology Browser
Joubert syndrome 3 (DOID:0110998)
Alliance: disease page
Synonyms: JBTS3
Alt IDs: OMIM:608629, MESH:C536295
Definition: A Joubert syndrome that has_material_basis_in homozygous mutation in the AHI1 gene on chromosome 6q23.3.

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
01/07/2020
MGI 6.14
The Jackson Laboratory