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DOID:0060171 - Dravet syndrome
Disease Ontology Definition:An epilepsy that is characterized by frequent febrile seizures with onset before 1 year.
Synonyms: SMEI, severe myoclonic epilepsy in infancy
OMIM:607208 - DRAVET SYNDROME; DRVT |
MONDO:0100135 - Dravet syndrome |
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s):
infancy electroclinical syndrome (is_a)