Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
Familial Adult Myoclonic Epilepsy, 1 (DOID:9003633)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
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 +   
Familial Adult Myoclonic Epilepsy, 1  
Familial Adult Myoclonic Epilepsy, 2  
Familial Adult Myoclonic Epilepsy, 3  
Familial Adult Myoclonic Epilepsy, 4  
Familial Adult Myoclonic Epilepsy, 5  
Familial Adult Myoclonic Epilepsy, 6  
Familial Adult Myoclonic Epilepsy, 7  
familial encephalopathy with neuroserpin inclusion bodies  
Feigenbaum Bergeron Richardson Syndrome 
Hydroxylysinuria 
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: BAFME1 ;   Benign Adult Familial Myoclonic Epilepsy 1 ;   CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 1 ;   Cortical Myoclonic Tremor With Epilepsy, Familial ;   Cortical Tremor, Familial ;   FAME1 ;   FCMTE1 ;   Myoclonic Epilepsy, Benign Adult Familial, Type 1
Primary IDs: MESH:C563399
Alternate IDs: OMIM:601068

paths to the root

NHLBI Logo

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