Disease: Migraine, Familial Hemiplegic, 3 ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Migraine, Familial Hemiplegic, 3
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
0.800 GeneticVariation UNIPROT Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations. 19332696 2009
Migraine, Familial Hemiplegic, 3
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
0.800 GeneticVariation UNIPROT The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online. 17397047 2007
Migraine, Familial Hemiplegic, 3
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
0.800 GeneticVariation UNIPROT Novel mutation confirms seizure locus SCN1A is also familial hemiplegic migraine locus FHM3. 18021921 2007
Migraine, Familial Hemiplegic, 3
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
0.800 GeneticVariation UNIPROT Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. 16054936 2005
Migraine, Familial Hemiplegic, 3
CUI: C1864987
Disease: Migraine, Familial Hemiplegic, 3
0.800 CausalMutation CLINVAR