SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Developmental disorder  5294002

Neurodevelopmental disorder  700364009

Developmental and epileptic encephalopathy  1275631007

Severe myoclonic epilepsy in infancy   230437002

SNOMED CT code


SNOMED code230437002
nameSevere myoclonic epilepsy in infancy
statusactive
date introduced2002-01-31
fully specified name(s)Severe myoclonic epilepsy in infancy (disorder)
synonyms
  • Severe myoclonic epilepsy in infancy
  • Dravet Syndrome
attributes - group1
Finding siteBrain structure   12738006
Pathological processPathological developmental process   308490002
OccurrenceInfancy   3658006
parentsDevelopmental and epileptic encephalopathy   1275631007
childrenSevere myoclonic epilepsy in infancy, refractory   432171000124102
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Neurodevelopmental disorder   700364009
          Developmental and epileptic encephalopathy   1275631007
            Severe myoclonic epilepsy in infancy   230437002

ancestors
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