8A61 Genetic or presumed genetic syndromes primarily expressed as epilepsy
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
The epilepsy is, as best as understood, the direct result of one or more known or presumed genetic defects in which seizures are the core symptom of the disorder.
sections/codes in this section (8A61-8A61)
- Genetic epileptic syndromes with neonatal onset (8A61.0)
- Genetic epileptic syndromes with onset in infancy (8A61.1)
- Genetic epileptic syndromes with childhood onset (8A61.2)
- Genetic epileptic syndrome with adolescent or adult onset (8A61.3)
- Genetic epileptic syndromes with variable age of onset (8A61.4)
- Other specified genetic or presumed genetic syndromes primarily expressed as epilepsy (8A61.Y)
- Genetic or presumed genetic syndromes primarily expressed as epilepsy, unspecified (8A61.Z)
postcoordination
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