Severe myoclonic epilepsy in infancy, refractory   432171000124102

SNOMED CT code


SNOMED code432171000124102
nameSevere myoclonic epilepsy in infancy, refractory
statusactive
date introduced2012-09-01
fully specified name(s)Severe myoclonic epilepsy in infancy, refractory (disorder)
synonyms
  • Severe myoclonic epilepsy in infancy, refractory
  • Severe myoclonic epilepsy in infancy, intractable
  • Dravet syndrome, refractory
  • Dravet syndrome, intractable
attributes - group1
OccurrenceInfancy   3658006
Finding siteBrain structure   12738006
Pathological processPathological developmental process   308490002
attributes - group2
Associated withDrug or medicament   410942007
parents
  • Drug resistance to anti-seizure medication   1263935000
  • Severe myoclonic epilepsy in infancy   230437002
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Drug resistance   31438003
        Drug resistance to anti-seizure medication   1263935000
          Severe myoclonic epilepsy in infancy, refractory   432171000124102

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
              Severe myoclonic epilepsy in infancy, refractory   432171000124102

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