SE-ATLAS

PEHO syndrome Distal duplication 15q Inverted duplicated chromosome 15 syndrome Rare epilepsy Moynahan syndrome CNTNAP2-related developmental and epileptic encephalopathy Oculocerebrocutaneous syndrome Sturge-Weber syndrome DEND syndrome Action myoclonus-renal failure syndrome Infantile spasms-broad thumbs syndrome Infantile epilepsy syndrome Neonatal epilepsy syndrome Adolescent-onset epilepsy syndrome Childhood-onset epilepsy syndrome Epilepsy syndrome Chromosomal anomaly with epilepsy as a major feature Neurocutaneous syndrome with epilepsy Monogenic disease with epilepsy W syndrome Idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes Metabolic diseases with epilepsy Cerebral malformation with epilepsy Inflammatory and autoimmune disease with epilepsy Infectious disease with epilepsy Cerebral diseases of vascular origin with epilepsy Atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome PEHO-like syndrome Succinic semialdehyde dehydrogenase deficiency CDKL5-deficiency disorder