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Ontology Browser

Term:
idiopathic generalized epilepsy 11 (DOID:0111312)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
childhood onset epileptic encephalopathy +   
generalized epilepsy with febrile seizures plus +   
idiopathic generalized epilepsy 10 +   
idiopathic generalized epilepsy 11  
An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the CLCN2 on chromosome 3q27.1. (DO)
idiopathic generalized epilepsy 12  
idiopathic generalized epilepsy 13  
idiopathic generalized epilepsy 14  
idiopathic generalized epilepsy 15  
Idiopathic Generalized Epilepsy 16  
idiopathic generalized epilepsy 2 
idiopathic generalized epilepsy 3 
idiopathic generalized epilepsy 4 
idiopathic generalized epilepsy 5 
idiopathic generalized epilepsy 7  
idiopathic generalized epilepsy 8  
idiopathic generalized epilepsy 9  
juvenile absence epilepsy 1  
juvenile myoclonic epilepsy 10  
juvenile myoclonic epilepsy 3 
juvenile myoclonic epilepsy 4 
juvenile myoclonic epilepsy 9 

Synonyms
Exact Synonyms: EIG11
Narrow Synonyms: EJA2 ;   EJM8
Related Synonyms: idiopathic generalized epilepsy, susceptibility to, 11 ;   juvenile absence epilepsy, susceptibility to, 2 ;   juvenile myoclonic epilepsy, susceptibility to, 8
Primary IDs: OMIM:607628
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/19710712 "DO"

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