Epilepsy, idiopathic generalized, susceptibility to, 13; EIG13

Disease ID:210
Name:Epilepsy, idiopathic generalized, susceptibility to, 13; EIG13
Associated with:1 target
Synonyms
Childhood absence epilepsy | Idiopathic generalized epilepsy | Juvenile myoclonic epilepsy
Description
The OMIM entry for this diseases also represents juvenile myoclonic epilepsy type 5, and childhood absence epilepsy type 4, as they have been classed as subtypes of idiopathic generalized epilepsy. Please see the OMIM entry for more detailed information.
Database Links
Disease Ontology: DOID:1827, DOID:1825
OMIM: 611136
Orphanet: ORPHA64280, ORPHA307

Targets

GABAA receptor α1 subunit

Ligands

No ligand related data available for Epilepsy, idiopathic generalized, susceptibility to, 13; EIG13