8A61.0 Genetic epileptic syndromes with neonatal onset
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Epilepsy with onset in the first 30 days of life resulting from one or more known or presumed genetic defects in which seizures are the core symptom of the disorder.
exclusions
sections/codes in this section (8A61.0-8A61.0)
- Pyridoxal dependent epilepsy (8A61.00)
- Other specified genetic epileptic syndromes with neonatal onset (8A61.0Y)
- Genetic epileptic syndromes with neonatal onset, unspecified (8A61.0Z)
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
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