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Disease Ontology Browser
Joubert syndrome 1 (DOID:0110980)
Alliance: disease page
Synonyms: cerebellooculorenal syndrome 1; cerebelloparenchymal disorder IV; CORS1; CPD4; JBTS1
Alt IDs: OMIM:213300
Definition: A Joubert syndrome that has_material_basis_in homozygous mutation in the INPP5E gene on chromosome 9q34.


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