IRF8, interferon regulatory factor 8, 3394

N. diseases: 149; N. variants: 20
Disease: SMITH-MCCORT DYSPLASIA 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3888088
Disease: SMITH-MCCORT DYSPLASIA 1
SMITH-MCCORT DYSPLASIA 1 		0.010 Biomarker disease BEFREE Altogether, IRF8 is crucial in modulating SMC phenotype switching and neointima formation in response to vascular injury via direct interaction with the SRF/myocardin complex. 24248596 2014