Dravet syndrome (DS) is a genetic epilepsy of childhood characterized by a variety of drug-resistant seizures often induced by fever, presenting in previously healthy children, and which frequently leads to cognitive and motor impairment.

Synonyms: SMEI Severe myoclonus epilepsy of infancy Severe myoclonic epilepsy of infancy DS

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Term information

database cross reference
hasDbXref

OMIM:607208
OMIM:612164
OMIM:615744
UMLS:C0751122
ICD-10:G40.4

notation

ORPHA:33069