FOXF2, forkhead box F2, 2295

N. diseases: 57; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0266121
Disease: Congenital absence of uvula
Congenital absence of uvula
0.010 Biomarker disease BEFREE Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family. 30917284 2019