SETBP1, SET binding protein 1, 26040

N. diseases: 257; N. variants: 28
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023014
Disease: Language Development Disorders
Language Development Disorders
0.310 Biomarker group BEFREE Several genes (including the candidate SETBP1 and other MEF2-related genes) seem to jointly influence certain, but not all, facets of the DLD phenotype. 27016271 2016
CUI: C0023014
Disease: Language Development Disorders
Language Development Disorders
0.310 Biomarker group CTD_human Refining analyses of copy number variation identifies specific genes associated with developmental delay. 25217958 2014