FOXF1, forkhead box F1, 2294

N. diseases: 135; N. variants: 7
Disease: Pyloric Stenosis, Hypertrophic ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0700639
Disease: Pyloric Stenosis, Hypertrophic
Pyloric Stenosis, Hypertrophic 		0.010 GeneticVariation disease BEFREE A novel missense mutation in the transcription factor FOXF1 cosegregating with infantile hypertrophic pyloric stenosis in the extended pedigree linked to IHPS5 on chromosome 16q24. 27855150 2017