FOXP2, forkhead box P2, 93986

N. diseases: 165; N. variants: 32
Disease: Russell-Silver syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0175693
Disease: Russell-Silver syndrome
Russell-Silver syndrome 		0.310 Biomarker disease BEFREE Our results indicate that absence of paternal FOXP2 is the cause of DVD in patients with SRS with maternal UPD7. 17033973 2006
CUI: C0175693
Disease: Russell-Silver syndrome
Russell-Silver syndrome 		0.310 Biomarker disease CTD_human Our results indicate that absence of paternal FOXP2 is the cause of DVD in patients with SRS with maternal UPD7. 17033973 2006