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Disease Ontology Browser
Joubert syndrome 20 (DOID:0110989)
Alliance: disease page
Synonyms: JBTS20
Alt IDs: OMIM:614970
Definition: A Joubert syndrome that has_material_basis_in compound heterozygous mutation in the TMEM231 gene on chromosome 16q23.


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