Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
0.110 GeneticVariation group BEFREE In addition, he has vertebral anomalies, brachymelia of the arms, and a ventricular septal defect-features that are reminiscent of Robinow syndrome, which has also been shown to be caused by mutations in ROR2. 10986040 2000
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
0.110 Biomarker group HPO