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Disease Ontology Browser
idiopathic generalized epilepsy 12 (DOID:0111313)
Alliance: disease page
Synonyms: EIG12
Alt IDs: OMIM:614847
Definition: An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC2A1 on chromosome 1p34.2.


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
02/18/2020
MGI 6.14
The Jackson Laboratory