Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.030 Biomarker disease BEFREE We confirmed the contribution to CHD of copy number changes in genes such as GATA4 and NODAL and identified several genes in novel recurrent CNVs that may point to novel CHD candidate loci. 23979609 2014
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.030 Biomarker disease BEFREE To our knowledge, this is the first study to suggest that NODAL may be involved in the etiology of nonsyndromic CHD in a Chinese population. 22352765 2012
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.030 GeneticVariation disease BEFREE Significant reductions in the biological activity of NODAL alleles are detected among patients with congenital heart defects (CHD), laterality anomalies (e.g. left-right mis-specification phenotypes), and only rarely holoprosencephaly (HPE). 19553149 2009