Epilepsy due to structural or metabolic conditions or diseases

Definition

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.

14 subordinate codes

• 8A60.0Epilepsy due to prenatal or perinatal brain insults
• 8A60.1Epilepsy due to cerebrovascular disorders
• 8A60.2Epilepsy due to degenerative brain disorders
• 8A60.3Epilepsy due to dementias
• 8A60.4Epilepsy due to central nervous system infections or infestations
• 8A60.5Epilepsy due to injuries to the head
• 8A60.6Epilepsy due to tumours of the nervous system
• 8A60.7Epilepsy with mesial temporal sclerosis
• 8A60.8Epilepsy due to immune disorders
• 8A60.9Epilepsy due to abnormalities of brain development
• 8A60.AEpilepsy due to genetic syndromes with widespread or progressive effects
• 8A60.BEpilepsy due to multiple sclerosis or other demyelinating disorders
• 4B4YOther specified diseases of the immune system
• 4B4ZDiseases of the immune system, unspecified

Nearby in Epilepsy or seizures

• 8A61Genetic or presumed genetic syndromes primarily expressed as epilepsy
• 8A62Epileptic encephalopathies
• 8A63Seizure due to acute causes
• 8A64Single seizure due to remote causes
• 8A65Single unprovoked seizure
• 8A66Status epilepticus
• 8A67Acute repetitive seizures
• 8A68Types of seizures