ICD-10: G40.844

early onset absence epilepsy early infantile epileptic encephalopathy X-linked monogenic disease rapadilino syndrome Kahrizi syndrome IMAGe syndrome episodic ataxia type 6 Baraitser-Winter syndrome Warburg micro syndrome Van Maldergem syndrome MASA syndrome oculodentodigital dysplasia CEDNIK syndrome Stormorken syndrome Vici syndrome orofaciodigital syndrome III orofaciodigital syndrome VIII orofaciodigital syndrome IX chromosome 17p13.1 deletion syndrome chromosome 17q21.31 duplication syndrome myoclonic-atonic epilepsy MEDNIK syndrome EAST syndrome Barber-Say syndrome lethal congenital contracture syndrome 1 3MC syndrome 3 Yunis-Varon syndrome lethal congenital contracture syndrome 4 autosomal dominant nocturnal frontal lobe epilepsy 2 autosomal dominant nocturnal frontal lobe epilepsy 4 familial temporal lobe epilepsy 3 familial temporal lobe epilepsy 4 familial temporal lobe epilepsy 2 hypomyelinating leukodystrophy 13 syndromic X-linked intellectual disability 17 syndromic X-linked intellectual disability 7 Christianson syndrome Pierson syndrome monogenic disease periventricular nodular heterotopia ABCD syndrome Bjornstad syndrome Borjeson-Forssman-Lehmann syndrome electroclinical syndrome infancy electroclinical syndrome variable age at onset electroclinical syndrome