Epilepsy, Idiopathic Generalized 13 (EIG13)

Alias:

Epilepsy, Childhood Absence 4

Epilepsy, Idiopathic Generalized, Susceptibility to, 13

Eig13

Epilepsy, Childhood Absence, Susceptibility to, 4

Idiopathic Generalized Epilepsy 13

Epilepsy, Idiopathic, Generalized, Susceptibility to, Type 13

Epilepsy, Juvenile Myoclonic, Susceptibility to, 5

Susceptibility to Juvenile Myoclonic Epilepsy 5

Epilepsy, Juvenile Myoclonic 5

Juvenile Myoclonic Epilepsy 5

Eca4

Ejm5

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Epilepsy, Idiopathic Generalized 13, also known as epilepsy, childhood absence 4, is related to mood disorder and angelman syndrome. An important gene associated with Epilepsy, Idiopathic Generalized 13 is GABRA1 (Gamma-Aminobutyric Acid Type A Receptor Subunit Alpha1). Affiliated tissues include brain, and related phenotype is reproductive system.

Related ID：

MALACARDS：EPL205

OMIM：611136

MESH：D004829