8A60ICD-11 MMS 2026-01
Epilepsy due to structural or metabolic conditions or diseases
Description
Epilepsy occurring in relation to a distinct other structural or metabolic condition or disease that has been demonstrated to be associated with a substantially increased risk of developing epilepsy.
Coding note from above levels
Use additional code, if desired, to identify the type of seizure.
Exclusions from above levels
Child codes
8A60.0– Epilepsy due to prenatal or perinatal brain insults8A60.1– Epilepsy due to cerebrovascular disorders8A60.2– Epilepsy due to degenerative brain disorders8A60.3– Epilepsy due to dementias8A60.4– Epilepsy due to central nervous system infections or infestations8A60.5– Epilepsy due to injuries to the head8A60.6– Epilepsy due to tumours of the nervous system8A60.7– Epilepsy with mesial temporal sclerosis8A60.8– Epilepsy due to immune disorders8A60.9– Epilepsy due to abnormalities of brain development8A60.A– Epilepsy due to genetic syndromes with widespread or progressive effects8A60.B– Epilepsy due to multiple sclerosis or other demyelinating disorders8A60.Y– Epilepsy due to other structural or metabolic condition or disease8A60.Z– Epilepsy due to unspecified structural or metabolic condition or disease
Sibling codes
8A61– Genetic or presumed genetic syndromes primarily expressed as epilepsy8A62– Epileptic encephalopathies8A63– Seizure due to acute causes8A64– Single seizure due to remote causes8A65– Single unprovoked seizure8A66– Status epilepticus8A67– Acute repetitive seizures8A68– Types of seizures8A6Y– Other specified epilepsy or seizures8A6Z– Epilepsy or seizures, unspecified
Foundation entity
Epilepsy due to structural or metabolic conditions or diseases – http://id.who.int/icd/entity/2073711696
Allowed postcoordination axes
Part of: 08: Diseases of the nervous system