WNT2, Wnt family member 2, 7472

N. diseases: 96; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0241210
Disease: Speech Delay
Speech Delay
0.010 GeneticVariation disease BEFREE The WNT2 gene polymorphism associated with speech delay inherent to autism. 22522212 2012