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8A61.2Y Other specified genetic epileptic syndromes with childhood onset International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2025-01 postcoordination Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Has manifestation - multiple selections are allowed [select] 8A68 Types of seizures – 8A68.0 Focal unaware seizure – 8A68.1 Absence seizures, atypical – 8A68.2 Absence seizures, typical – 8A68.3 Focal aware seizure – 8A68.4 Generalised tonic-clonic seizure – 8A68.5 Generalised myoclonic seizure – 8A68.6 Generalised tonic seizure – 8A68.7 Generalised atonic seizure – 8A68.Y Other specified type of seizure – 8A68.Z Type of seizure, unspecified
synonyms Other specified genetic epileptic syndromes with childhood onset Generalised epilepsy - paroxysmal dyskinesia Generalised epilepsy with febrile seizures plus Benign occipital epilepsy Early onset benign occipital epilepsy, Panayiotopoulos type Panayiotopoulos syndrome Late onset childhood occipital epilepsy, Gastaut type Idiopathic childhood occipital epilepsy of Gastaut Myoclonic epilepsy in early childhood Epilepsy with myoclonic-atonic seizures Perioral myoclonia with absences Jeavons syndrome Cryptogenic late-onset epileptic spasms Rolandic epilepsy-speech dyspraxia syndrome Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
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