Epilepsy, Idiopathic Generalized 10 (EIG10)

Alias:

Epilepsy, Idiopathic Generalized, Susceptibility to, 10

Eig10

Generalized Epilepsy with Febrile Seizures Plus, Type 5

Generalized Epilepsy with Febrile Seizures Plus Type 5

Epilepsy, Juvenile Myoclonic, Susceptibility to

Epilepsy, Idiopathic Generalized, 10

Idiopathic Generalized Epilepsy 10

Epilepsy, Juvenile Myoclonic 7

Generalized Epilepsy with Febrile Seizures Plus, Type 5, Susceptibility to

Epilepsy, Idiopathic, Generalized, Susceptibility to, Type 10

Susceptibility to Idiopathic Generalized Epilepsy 10

Generalized Epilepsy with Febrile Seizures Plus 5

Susceptibility to Juvenile Myoclonic Epilepsy 7

Juvenile Myoclonic Epilepsy 7

Myoclonic Epilepsy, Juvenile

Epilepsy, Juvenile Myoclonic

Gefs+ Type 5

Gefsp5

Gefs+5

Ejm7

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Epilepsy, Idiopathic Generalized 10, also known as epilepsy, idiopathic generalized, susceptibility to, 10, is related to epilepsy, idiopathic generalized 11 and childhood absence epilepsy, and has symptoms including myoclonus and absence seizures. An important gene associated with Epilepsy, Idiopathic Generalized 10 is GABRD (Gamma-Aminobutyric Acid Type A Receptor Subunit Delta). Affiliated tissues include brain and temporal lobe, and related phenotypes are generalized myoclonic seizure and bilateral tonic-clonic seizure

Related ID：

MALACARDS：EPL209

OMIM：613060

MESH：D003294