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8A68 Types of seizures International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01 exclusions sections/codes in this section (8A68-8A68) postcoordination Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has causing condition - a selection is required - multiple selections are allowed [select] 8A60 Epilepsy due to structural or metabolic conditions or diseases – 8A60.0 Epilepsy due to prenatal or perinatal brain insults – 8A60.1 Epilepsy due to cerebrovascular disorders – 8A60.2 Epilepsy due to degenerative brain disorders – 8A60.3 Epilepsy due to dementias – 8A60.4 Epilepsy due to central nervous system infections or infestations – 8A60.5 Epilepsy due to injuries to the head – 8A60.6 Epilepsy due to tumours of the nervous system – 8A60.7 Epilepsy with mesial temporal sclerosis – 8A60.8 Epilepsy due to immune disorders – 8A60.9 Epilepsy due to abnormalities of brain development – 8A60.A Epilepsy due to genetic syndromes with widespread or progressive effects – 8A60.B Epilepsy due to multiple sclerosis or other demyelinating disorders – 8A60.Y Epilepsy due to other structural or metabolic condition or disease – 8A60.Z Epilepsy due to unspecified structural or metabolic condition or disease –– 8A60.00 Epilepsy due to prenatal or perinatal vascular insults –– 8A60.01 Epilepsy due to neonatal hypoxic ischemic encephalopathy –– 8A60.0Y Epilepsy due to other prenatal or perinatal brain insults –– 8A60.0Z Epilepsy due to unspecified prenatal or perinatal brain insults 8A61 Genetic or presumed genetic syndromes primarily expressed as epilepsy – 8A61.0 Genetic epileptic syndromes with neonatal onset – 8A61.1 Genetic epileptic syndromes with onset in infancy – 8A61.2 Genetic epileptic syndromes with childhood onset – 8A61.3 Genetic epileptic syndrome with adolescent or adult onset – 8A61.4 Genetic epileptic syndromes with variable age of onset – 8A61.Y Other specified genetic or presumed genetic syndromes primarily expressed as epilepsy – 8A61.Z Genetic or presumed genetic syndromes primarily expressed as epilepsy, unspecified –– 8A61.00 Pyridoxal dependent epilepsy –– 8A61.0Y Other specified genetic epileptic syndromes with neonatal onset –– 8A61.0Z Genetic epileptic syndromes with neonatal onset, unspecified –– 8A61.10 Benign familial infantile epilepsy –– 8A61.11 Dravet syndrome –– 8A61.12 Epilepsy of infancy with migrating focal seizures –– 8A61.1Y Other specified genetic epileptic syndromes with onset in infancy –– 8A61.1Z Genetic epileptic syndromes with onset in infancy, unspecified –– 8A61.20 Benign childhood epilepsy with centro-temporal spikes –– 8A61.21 Childhood absence epilepsy –– 8A61.22 Epilepsy with myoclonic-astatic seizures –– 8A61.23 Myoclonic absences or absences with myoclonias –– 8A61.2Y Other specified genetic epileptic syndromes with childhood onset –– 8A61.2Z Genetic epileptic syndromes with childhood onset, unspecified –– 8A61.30 Juvenile myoclonic epilepsy –– 8A61.31 Juvenile absence epilepsy –– 8A61.32 Benign adult familial myoclonus epilepsy –– 8A61.3Y Other specified genetic epileptic syndrome with adolescent or adult onset –– 8A61.3Z Genetic epileptic syndrome with adolescent or adult onset, unspecified –– 8A61.40 Reflex epilepsies –– 8A61.41 Progressive myoclonic epilepsy –– 8A61.4Y Other specified genetic epileptic syndromes with variable age of onset –– 8A61.4Z Genetic epileptic syndromes with variable age of onset, unspecified 8A62 Epileptic encephalopathies – 8A62.0 Infantile spasms – 8A62.1 Lennox-Gastaut syndrome – 8A62.2 Acquired epileptic aphasia – 8A62.Y Other specified epileptic encephalopathies – 8A62.Z Epileptic encephalopathies, unspecified 8A63 Seizure due to acute causes – 8A63.0 Febrile seizures – 8A63.Y Seizure due to other acute cause – 8A63.Z Seizure due to unspecified acute cause –– 8A63.00 Simple febrile seizures –– 8A63.01 Complex febrile seizures –– 8A63.0Y Other specified febrile seizures –– 8A63.0Z Febrile seizures, unspecified
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