FOXF1, forkhead box F1, 2294

N. diseases: 135; N. variants: 7
Disease: Amyloidosis cutis dyschromia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4554601
Disease: Amyloidosis cutis dyschromia
Amyloidosis cutis dyschromia 		0.020 GeneticVariation disease BEFREE Rapid mutation analysis in FOXF1 may provide noninvasive early confirmation of ACD in neonates with respiratory failure and can aid in clinical decision making. 25627281 2015
CUI: C4554601
Disease: Amyloidosis cutis dyschromia
Amyloidosis cutis dyschromia 		0.020 AlteredExpression disease BEFREE We also found decreased expression of Forkhead box protein F1 (Foxf1), a gene associated with the ACD human phenotype. 23023706 2012