Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0476254
Disease: Dyslexia
Dyslexia
0.010 GeneticVariation disease BEFREE Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. 20346443 2010