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Disease Ontology Browser
Dravet syndrome (DOID:0080422)
Alliance: disease page
Synonyms: DEE6; DEE6A; developmental and epileptic encephalopathy 6; developmental and epileptic encephalopathy 6A; early infantile epileptic encephalopathy 6; severe myoclonic epilepsy of infancy
Alt IDs: OMIM:607208, ORDO:33069
Definition: A developmental and epileptic encephalopathy characterized by onset of seizures that are usually refractory to treatment in the first year of life after normal early development and impaired psychomoter development starting around the second year of life that has_material_basis_in heterozygous mutation in the SCN1A gene on chromosome 2q24.

Disease References using Mouse Models (28)
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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12/10/2024
MGI 6.24 		The Jackson Laboratory