NEURO disease 924


disease_name
{Epilepsy, idiopathic generalized}, 600669 (2)
disease_id
600669
gene_name
EIG2
Ensembl_id
-
gene_mol_descr
-
gene_id
606972
location
14q23
disease_type
NEURO
cs
INHERITANCE: Autosomal dominant NEUROLOGIC: [Central nervous system]; Generalized seizures, recurrent; Generalized tonic-clonic seizures; Absence seizures; Myoclonic seizures; EEG shows generalized, bilateral, synchronous, symmetrical discharge; EEG shows spike and multispike waves, 3-4 Hz MISCELLANEOUS: Comprises several subtypes, including; Benign neonatal familial convulsions (see 601764, 121200, 121201, and 269720); Childhood absence epilepsy (ECA1 600131, ECA2 607681, ECA3 607682); Juvenile absence epilepsy (JAE, 607631); Juvenile myoclonic epilepsy (JME, 606904); Epilepsy with grand mal seizures on awakening (EGMA, 607628)
mouse_ortholog
-
mouse_phenotype
-