FOXF1, forkhead box F1, 2294

N. diseases: 135; N. variants: 7
Disease: Congenital anomaly of gastrointestinal tract ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0012241
Disease: Congenital anomaly of gastrointestinal tract
Congenital anomaly of gastrointestinal tract 		0.010 GeneticVariation group BEFREE Here, we describe monozygotic twins and one full-term newborn with ACD and gastrointestinal malformations caused by de novo mutations of FOXF1 on the maternal-inherited alleles. 28256047 2017