Genetic epileptic syndromes with childhood onset, 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

8A61.20 – Benign childhood epilepsy with centro-temporal spikes
8A61.21 – Childhood absence epilepsy
8A61.22 – Epilepsy with myoclonic-astatic seizures
8A61.23 – Myoclonic absences or absences with myoclonias
8A61.2Y – Other specified genetic epileptic syndromes with childhood onset

Foundation entity

Genetic epileptic syndromes with childhood onset – http://id.who.int/icd/entity/1612372804

Allowed postcoordination axes

hasManifestation

Part of: 8A61.2: Genetic epileptic syndromes with childhood onset › 8A61: Genetic or presumed genetic syndromes primarily expressed as epilepsy › 08: Diseases of the nervous system