MGR6, Migraine, several forms, 317773

N. diseases: 5; N. variants: 0
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0036572
Disease: Seizures
Seizures
0.010 GeneticVariation phenotype BEFREE Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3. 18021921 2007