Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		0.020 AlteredExpression BEFREE Elevated synthesis of fibronectin in the calvaria of patients with Apert syndrome and increased fibronectin gene expression in port wine-derived fibroblasts of patients with Sturge-Weber disease have also been reported. 29476210

2018
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		0.020 Biomarker BEFREE The phenotype of cultured fibroblasts from patients affected by Apert's syndrome, a rare connective disorder, differs from that of normal cells in its extracellular matrix macromolecule composition (glycosaminoglycans, collagens and fibronectin) and is further modulated by treatment with interleukins (ILs). 9628325

1998