166463 Epilepsy syndrome 4

166466 Neurocutaneous syndrome with epilepsy

166469 Chromosomal anomaly with epilepsy as a major feature

166472 Monogenic disease with epilepsy 4

166475 Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes 1

166478 Cerebral malformation with epilepsy 3

166481 Metabolic diseases with epilepsy 9

166484 Inflammatory and autoimmune disease with epilepsy 2

166487 Cerebral diseases of vascular origin with epilepsy

166490 Infectious disease with epilepsy