8A61 Genetic or presumed genetic syndromes primarily expressed as epilepsy

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2025-01

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 ()

• 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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