Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751529
Disease: Stuttering, Developmental
Stuttering, Developmental
0.310 Biomarker phenotype BEFREE A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering. 24807205 2014
CUI: C0751529
Disease: Stuttering, Developmental
Stuttering, Developmental
0.310 Biomarker phenotype CTD_human Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering case. 21108403 2010