Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.420 GeneticVariation group BEFREE At one extreme, SNPs rs6790925 (near TGFBR2) and rs2274316 (MEF2D) were not associated with migraine overall, MA, or MO but were selective for migraine sub-classified by the presence of one or more of the additional migraine features. 24852292 2014
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.420 GeneticVariation group BEFREE On the other hand, TRPM8 rs10166942 and TGFBR2 rs7640543 variants did not have significant influence on migraine susceptibility in the North Indian population. 24266335 2014
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.420 Biomarker group CTD_human Clinical features in a family with an R460H mutation in transforming growth factor beta receptor 2 gene. 16885183 2006
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.420 Biomarker group HPO