Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2349453
Disease: Familial migraine
Familial migraine
0.010 GeneticVariation disease BEFREE Mutations in the NaV1.1 neuronal sodium channel alpha-subunit (SCN1A) gene have been documented in a spectrum of epilepsy syndromes, ranging from the relatively benign generalized epilepsy with febrile seizures plus (GEFS(+)) to severe myoclonic epilepsy in infancy (SMEI), and rare cases of familial migraine. 19469841 2009