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Disease Ontology Browser
early infantile epileptic encephalopathy 59 (DOID:0080291)
Alliance: disease page
Alt IDs: OMIM:617904
Definition: An early infantile epileptic encephalopathy that has_material_basis_in heterozygous mutation in the GABBR2 gene on chromosome 9q22.


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