Genetic epileptic syndromes with onset in infancy, unspecified

Coding note from above levels

Use additional code, if desired, to identify the type of seizure.

Exclusions from above levels

MG45 – Syncope
05 – Endocrine, nutritional or metabolic diseases
18 – Complications of pregnancy, childbirth and the puerperium

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19 – Certain conditions originating in the perinatal period
22 – Injury, poisoning or certain other consequences of external causes

Sibling codes

8A61.10 – Benign familial infantile epilepsy
8A61.11 – Dravet syndrome
8A61.12 – Epilepsy of infancy with migrating focal seizures
8A61.1Y – Other specified genetic epileptic syndromes with onset in infancy

Foundation entity

Genetic epileptic syndromes with onset in infancy – http://id.who.int/icd/entity/1310497511

Allowed postcoordination axes

hasManifestation

Part of: 8A61.1: Genetic epileptic syndromes with onset in infancy › 8A61: Genetic or presumed genetic syndromes primarily expressed as epilepsy › 08: Diseases of the nervous system