MEF2D, myocyte enhancer factor 2D, 4209

N. diseases: 72; N. variants: 10
Disease: Common Migraine ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0338480
Disease: Common Migraine
Common Migraine 		0.330 GeneticVariation disease BEFREE Sixteen of the patients were carriers of the risk allele rs2274316 ( MEF2D), which confers increased risk of MO and may regulate PACAP38 expression, and 16 were non-carriers. 26994298 2017
CUI: C0338480
Disease: Common Migraine
Common Migraine 		0.330 Biomarker disease BEFREE MEF2D, PRDM16 and ASTN2 were also found to be associated with migraine without aura (MO) and migraine with family history. 28058730 2017
CUI: C0338480
Disease: Common Migraine
Common Migraine 		0.330 GeneticVariation disease BEFREE Conclusion Migraine response to PACAP38 infusion in migraine without aura patients is not associated with high family load or the risk allele of rs2274316 ( MEF2D). 26994299 2017
CUI: C0338480
Disease: Common Migraine
Common Migraine 		0.330 Biomarker disease CTD_human Genome-wide association analysis identifies susceptibility loci for migraine without aura. 22683712 2012