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Ontology Browser

benign epilepsy with centrotemporal spikes (DOID:3329)
Annotations: Rat: (36) Mouse: (36) Human: (41) Chinchilla: (36) Bonobo: (35) Dog: (35) Squirrel: (34) Pig: (36)
Parent Terms Term With Siblings Child Terms
benign epilepsy with centrotemporal spikes +   
An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and dysarthria. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41)
childhood absence epilepsy +   
complex partial epilepsy  
early onset absence epilepsy 
Familial Focal Epilepsy, with Variable Foci 1  
Familial Focal Epilepsy, with Variable Foci 2  
Familial Focal Epilepsy, with Variable Foci 3  
Familial Focal Epilepsy, with Variable Foci 4  
Focal Epilepsy with Speech Disorder and with or without Mental Retardation  
frontal lobe epilepsy +   
Landau-Kleffner syndrome  
Lennox-Gastaut syndrome  
Partial Epilepsy with Pericentral Spikes 
partial motor epilepsy  
partial sensory epilepsy +  
simple partial epilepsy 
temporal lobe epilepsy +   

Exact Synonyms: BCECTS ;   BECTS ;   Benign Childhood Epilepsy With Centro Temporal Spikes ;   Benign Epilepsy Of Childhood With Centrotemporal Spikes ;   Benign Rolandic Epilepsy ;   Benign Rolandic Epilepsy of Childhood ;   Centralopathic Epilepsies ;   Centralopathic Epilepsy ;   Centrotemporal Epilepsies ;   Centrotemporal Epilepsy ;   ECT ;   Rolandic Epilepsies ;   Rolandic Epilepsy ;   Rolands Epilepsy ;   Sylvian Epilepsy ;   Temporal-Central Focal Epilepsy ;   benign childhood epilepsy with centrotemporal spike ;   sylvan seizures
Primary IDs: MESH:D019305 ;   RDO:0000639
Alternate IDs: OMIM:117100
Definition Sources: MESH:D019305

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.