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Disease Ontology Browser
developmental and epileptic encephalopathy 32 (DOID:0080416)
Alliance: disease page
Synonyms: DEE32; early infantile epileptic encephalopathy 32
Alt IDs: OMIM:616366
Definition: A developmental and epileptic encephalopathy characterized by seizure onset between 5 and 17 months of age resulting in residual neurologic deficits; in some patients seizures may remit or respond to drug treatment, and that has_material_basis_in heterozygous mutation in the KCNA2 gene on chromosome 1p13.

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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
MGI 6.22
The Jackson Laboratory