RUNX2, RUNX family transcription factor 2, 860

N. diseases: 405; N. variants: 37
Disease: Heterotopic Ossification ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0029396
Disease: Heterotopic Ossification
Heterotopic Ossification 		0.210 Biomarker phenotype RGD Runx2 and Smad4 independently inhibited the formation of heterotopic ossification. 19940863 2010
CUI: C0029396
Disease: Heterotopic Ossification
Heterotopic Ossification 		0.210 Biomarker phenotype LHGDN A functional RNAi screen for Runx2-regulated genes associated with ectopic bone formation in human spinal ligaments. 18319563 2008