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Disease Ontology Browser
chromosome 2q31.2 deletion syndrome (DOID:0060416)
Alliance: disease page
Alt IDs: OMIM:612345, MESH:C567344
Definition: A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 2q31.2 region.


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
11/12/2024
MGI 6.24
The Jackson Laboratory