Familial hemiplegic migraine

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
familial hemiplegic migraine
MONDO_0018925MONDO_0012320
CACNA1A Causal
17575281 21734179 29442233 8734765 12756131 20682717 27250579 24836863 11439943 18400034 11409427 10408532 8898206 26716990 28900389 15032980 14718690 29053796
Open Targets
SCN1A Causal
10742094 11359211 16054936 17397047 18021921 19332696 28794249 33712547
ClinGen, Open Targets
All2 Causal2 Unknown0
Related Diseases Diseases that share the most curated genes with Familial hemiplegic migraine.
5 View disease cluster →
Benign paroxysmal torticollis of infancy 1 shared geneCACNA1A Related via 1 shared gene including CACNA1A. Hemiplegic migraine 2 shared genesCACNA1A, SCN1A Related via 2 shared genes including CACNA1A, SCN1A. Migraine, familial hemiplegic, 1, with progressive cerebellar ataxia 1 shared geneCACNA1A Related via 1 shared gene including CACNA1A. Febrile seizures, familial, 3a 1 shared geneSCN1A Related via 1 shared gene including SCN1A. Epileptic encephalopathy, early infantile, 6 (dravet syndrome) 1 shared geneSCN1A Related via 1 shared gene including SCN1A.