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Ontology Browser

Term:
familial adult myoclonic epilepsy (DOID:0111689)
Annotations: Rat: (7) Mouse: (7) Human: (7) Chinchilla: (7) Bonobo: (7) Dog: (7) Squirrel: (7) Pig: (7)
Parent Terms Term With Siblings Child Terms
Ataxia with Myoclonic Epilepsy and Presenile Dementia 
Congenital Deafness and Familial Myoclonic Epilepsy 
Dravet syndrome  
early myoclonic encephalopathy +   
epilepsy with generalized tonic-clonic seizures +   
familial adult myoclonic epilepsy +   
An adolescence-adult electroclinical syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities. (DO)
familial encephalopathy with neuroserpin inclusion bodies  
Feigenbaum Bergeron Richardson Syndrome 
Hydroxylysinuria 
juvenile absence epilepsy +   
juvenile myoclonic epilepsy +   
Myoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders 
Myoclonic Epilepsy, Familial Infantile  
Myoclonic Epilepsy, Hartung Type 
Myoclonic-Atonic Epilepsy  
Photoparoxysmal Response 3 
progressive myoclonus epilepsy +   
Spastic Paraplegia with Myoclonic Epilepsy 

Synonyms
Exact Synonyms: ADCME ;   BAFME ;   FAME ;   FCMTE ;   FMCTE ;   autosomal dominant cortical myoclonus and epilepsy ;   benign adult familial myoclonic epilepsy ;   benign adult familial myoclonus epilepsy ;   familial cortical myoclonic tremor and epilepsy
Xrefs: OMIM:PS601068 ;   ORDO:86814
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/20548044 "DO"

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