Seizure disorder   128613002

SNOMED CT code


SNOMED code128613002
nameSeizure disorder
statusactive
date introduced2002-01-31
fully specified name(s)Seizure disorder (disorder)
synonymsSeizure disorder
attributes - group1
Finding siteBrain structure   12738006
parents
children
  • 5q31.3 microdeletion syndrome   768555009
  • Aicardi's syndrome   80651009
  • Cyclin-dependent kinase-like 5 deficiency   773230003
  • Dissociative convulsions   191714002
  • Eclampsia   15938005
  • Epilepsy   84757009
  • Epileptic vertigo   68761002
  • Familial febrile convulsions   230432008
  • Familial neonatal seizures   279953009
  • Generalized-onset seizures   4619009  removed: 2021-09-30
  • Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome   1172630000
  • GM3 synthase deficiency   722762005
  • Intellectual disability, epilepsy, extrapyramidal syndrome   1187210007
  • Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome   770755007
  • ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement   1208747005
  • Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome   1187304005
  • Microcephaly, seizure, intellectual disability, heart disease syndrome   723304001
  • Multiple congenital anomalies, hypotonia, seizures syndrome   785303004
  • Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome   1217381009
  • Non-convulsive status epilepticus with three per second spike wave   230457003
  • Non-convulsive status epilepticus without three per second spike wave   230458008
  • Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome   722110003
  • Pachygyria, intellectual disability, epilepsy syndrome   763861000
  • Pitt-Hopkins syndrome   702344008
  • Primary hyperaldosteronism, seizures, neurological abnormalities syndrome   789063000
  • Primary hypomagnesemia, refractory seizures, intellectual disability syndrome   1269236003
  • Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome   442511009
  • Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome   770678005
  • PURA syndrome   768473009
  • Recurrent seizure   460731000124105
  • Refractory infantile spasms   422527005
  • Seizure co-occurrent and due to drug withdrawal   735235000  removed: 2022-10-31
  • Seizure co-occurrent and due to substance withdrawal   1254960008
  • Seizure disorder as sequela of stroke   137991000119103
  • Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome   721207002
  • Seizures complicating intracranial hemorrhage in the newborn   371107004
  • Seizures due to metabolic disorder   371022006
  • Seizures, scoliosis, macrocephaly syndrome   1187250005
  • Situation-related seizures   230431001
  • Unclassified epileptic seizures   77450009  removed: 2019-01-31
  • X-linked intellectual disability with seizure and psoriasis syndrome   719810000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Finding of brain   299718000
        Disorder of brain   81308009
          Seizure disorder   128613002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Finding of brain   299718000
        Seizure   91175000
          Seizure disorder   128613002

ancestors
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