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Dravet syndrome

^ http://www.orpha.net/ORDO/Orphanet_33069


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

Term info

database cross reference
  • ICD-10:G40.4 (Attributed)
  • UMLS:C0751122 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:607208 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:612164 (BTNT (broader term maps to a narrower term))
  • OMIM:615744 (BTNT (broader term maps to a narrower term))
  • ICD-10:G40.4 (NTBT (narrower term maps to a broader term))
hasDbXref

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

notation

ORPHA:33069