RUNX2, RUNX family transcription factor 2, 860

N. diseases: 405; N. variants: 37
Disease: Fibrous Dysplasia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0259779
Disease: Fibrous Dysplasia
Fibrous Dysplasia 		0.020 Biomarker disease BEFREE The CREB-Smad6-Runx2 axis contributes to the impaired osteogenesis potential of bone marrow stromal cells in fibrous dysplasia of bone. 22450860 2012
CUI: C0259779
Disease: Fibrous Dysplasia
Fibrous Dysplasia 		0.020 AlteredExpression disease BEFREE Fibroblastic cells in fibrous dysplasia and ossifying fibroma showed strong Runx2 expression in the nucleus. 17334331 2007