8A61.2 Genetic epileptic syndromes with childhood onset
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
sections/codes in this section (8A61.2-8A61.2)
- Benign childhood epilepsy with centro-temporal spikes (8A61.20)
- Childhood absence epilepsy (8A61.21)
- Epilepsy with myoclonic-astatic seizures (8A61.22)
- Myoclonic absences or absences with myoclonias (8A61.23)
- Other specified genetic epileptic syndromes with childhood onset (8A61.2Y)
- Genetic epileptic syndromes with childhood onset, unspecified (8A61.2Z)
postcoordination
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