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Disease Ontology Browser
Joubert syndrome 6 (DOID:0111001)
Alliance: disease page
Synonyms: JBTS6
Alt IDs: OMIM:610688, MESH:C537689
Definition: A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM67 on chromosome 8q22.

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
01/14/2020
MGI 6.14
The Jackson Laboratory