SE-ATLAS

Adolescent-onset epilepsy syndrome Childhood-onset epilepsy syndrome Neurocutaneous syndrome with epilepsy Epilepsy syndrome Chromosomal anomaly with epilepsy as a major feature Angelman syndrome Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Ring chromosome 14 syndrome W syndrome Monogenic disease with epilepsy Cerebral malformation with epilepsy Ring chromosome 20 syndrome Williams syndrome Metabolic diseases with epilepsy Cerebral diseases of vascular origin with epilepsy Inflammatory and autoimmune disease with epilepsy Infectious disease with epilepsy Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome PEHO-like syndrome PEHO syndrome Rare epilepsy Moynahan syndrome Kleefstra syndrome due to 9q34 microdeletion Smith-Magenis syndrome Oculocerebrocutaneous syndrome CNTNAP2-related developmental and epileptic encephalopathy Action myoclonus-renal failure syndrome DEND syndrome Infantile spasms-broad thumbs syndrome Angelman syndrome due to paternal uniparental disomy of chromosome 15 Angelman syndrome due to maternal 15q11q13 deletion 15q13.3 microdeletion syndrome Infantile epilepsy syndrome Neonatal epilepsy syndrome