Disease: Meningomyelocele ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Meningomyelocele
CUI: C0025312
Disease: Meningomyelocele
0.010 GeneticVariation BEFREE In addition, we also show a positive association between the SNP rs4846049 in the 3'-untranslated region of the MTHFR gene and the attention-deficit hyperactivity disorder phenotype in myelomeningocele participants. 23227261 2012