Migraine, familial basilar

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Subtype of: Migraine
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Migraine, familial basilar
MONDO_0011232
ATP1A2 Causal
12539047 12953268 15159495 15286158 18028407 18056581 19838529 21352219 23838748 23918834 25411546 25948653 28058944 28811059 29610157 30423015 30690204 31608932 33880529 37870493 38549198 39046620
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Migraine, familial basilar.
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Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies 1 shared geneATP1A2 Related via 1 shared gene including ATP1A2. Hemiplegic migraine-developmental and epileptic encephalopathy spectrum 1 shared geneATP1A2 Related via 1 shared gene including ATP1A2. Neuronal migration disorder with epilepsy 1 shared geneATP1A2 Related via 1 shared gene including ATP1A2. Coma 1 shared geneATP1A2 Related via 1 shared gene including ATP1A2. Benign familial infantile convulsions 1 shared geneATP1A2 Related via 1 shared gene including ATP1A2.