Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 146
Gene Symbol: ADRA1D
ADRA1D
0.030 GeneticVariation disease BEFREE Mutations involving the voltage-gated sodium channel alpha(I) gene SCN1A are major genetic causes of childhood epileptic disorders, as typified by Dravet syndrome. 20506560 2010
Entrez Id: 146
Gene Symbol: ADRA1D
ADRA1D
0.030 GeneticVariation disease BEFREE Mutations in SCN1A, the gene encoding the brain voltage-gated sodium channel alpha(1) subunit (Na(V)1.1), are associated with genetic forms of epilepsy, including generalized epilepsy with febrile seizures plus (GEFS+ type 2), severe myoclonic epilepsy of infancy (SMEI) and related conditions. 16210358 2005
Entrez Id: 146
Gene Symbol: ADRA1D
ADRA1D
0.030 GeneticVariation disease BEFREE Mutations in SCN1A, the gene encoding the brain voltage-gated sodium channel alpha(1) subunit (Na(V)1.1), are associated with at least two forms of epilepsy, generalized epilepsy with febrile seizures plus and severe myoclonic epilepsy of infancy (SMEI). 15263074 2004