Gene: ROR2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4920
Gene Symbol: ROR2
ROR2 		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
Entrez Id: 4920
Gene Symbol: ROR2
ROR2 		0.110 Biomarker group HPO