8A61
Genetic or presumed genetic syndromes primarily expressed as epilepsy
Genetic or presumed genetic syndromes primarily expressed as epilepsy
Child Codes (7)
8A61.0Genetic epileptic syndromes with neonatal onset
8A61.1Genetic epileptic syndromes with onset in infancy
8A61.2Genetic epileptic syndromes with childhood onset
8A61.3Genetic epileptic syndrome with adolescent or adult onset
8A61.4Genetic epileptic syndromes with variable age of onset
8A61.YOther specified genetic or presumed genetic syndromes primarily expressed as epilepsy
8A61.ZGenetic or presumed genetic syndromes primarily expressed as epilepsy, unspecified
Frequently Asked Questions
What is the ICD-11 code for genetic or presumed genetic syndromes primarily expressed as epilepsy?
The ICD-11 code for genetic or presumed genetic syndromes primarily expressed as epilepsy is 8A61. The full clinical description is "Genetic or presumed genetic syndromes primarily expressed as epilepsy".
What does ICD-11 code 8A61 mean?
ICD-11 code 8A61 represents “Genetic or presumed genetic syndromes primarily expressed as epilepsy”. It is classified under Chapter 8: Diseases of the Nervous System.
What chapter is 8A61 in?
8A61 is in Chapter 8: Diseases of the Nervous System (codes 8A00-8E7Z).
What is the ICD-10 equivalent of ICD-11 code 8A61?
There is no direct ICD-10 mapping available for 8A61 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-10. Use the ICD-11 to ICD-10 converter to search for related codes.
What is the difference between ICD-10 and ICD-11?
ICD-11 is the latest revision of the WHO's International Classification of Diseases, succeeding ICD-10. Key differences include: a fully digital-first design, new chapters for sleep-wake disorders, sexual health, and traditional medicine, improved coding for rare diseases, and better integration with electronic health records through extension codes.
What are the subcategories under 8A61?
8A61 has 7 child codes, including: 8A61.0 (Genetic epileptic syndromes with neonatal onset), 8A61.1 (Genetic epileptic syndromes with onset in infancy), 8A61.2 (Genetic epileptic syndromes with childhood onset), 8A61.3 (Genetic epileptic syndrome with adolescent or adult onset), and 3 more.
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