Disease Summary help help Associated Targets (144)Tbio81Tclin33Tchem29Tdark1 Explore Associated Targets list Mondo Term and Equivalent IDs MONDO:0015653: monogenic epilepsy Orphanet:166472: UMLS:CN200063: open_in_new
Disease Hierarchy help helpParentsepilepsy (1176)Tbio773Tchem195Tclin164Tdark44motor stereotypies (181)Tbio109Tchem34Tclin33Tdark5Childrenchannelopathy with epilepsy (126)Tbio65Tclin33Tchem27Tdark1familial infantile myoclonic epilepsy (10)Tbio8Tclin2Pitt-Hopkins syndrome (4)Tbio4autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome (4)Tbio3Tchem1X-linked intellectual disability-epilepsy syndrome (3)Tbio3Pitt-Hopkins-like syndrome (3)Tbio3Mowat-Wilson syndrome (1)Tbio1X-linked epilepsy-learning disabilities-behavior disorders syndrome (1)Tbio1severe neonatal-onset encephalopathy with microcephaly (1)Tchem1neuronal ceroid lipofuscinosis 8 northern epilepsy variant (1)Tbio1polyhydramnios, megalencephaly, and symptomatic epilepsy (1)Tbio1lethal neonatal spasticity-epileptic encephalopathy syndrome (1)Tbio1spastic paraplegia-severe developmental delay-epilepsy syndrome (1)Tbio1ARX-related epileptic encephalopathy (1)Tbio1neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination (1)Tbio1intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies (1)Tbio1FOXG1 disorder (1)Tbio1focal epilepsy-intellectual disability-cerebro-cerebellar malformation (0)infantile-onset mesial temporal lobe epilepsy with severe cognitive regression (0)global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome (0)PUM1-associated developmental disability-ataxia-seizure syndrome (0)