FN1, fibronectin 1, 2335

N. diseases: 724; N. variants: 33
Disease: Connective Tissue Diseases ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009782
Disease: Connective Tissue Diseases
Connective Tissue Diseases 		0.020 GeneticVariation group BEFREE We report on the preferential recruitment of the αvβ3 integrin, due to the lack of FN-ECM and its canonical integrin receptor, in dermal fibroblasts from Ehlers-Danlos syndromes (EDS) and arterial tortuosity syndrome (ATS), which are rare multisystem connective tissue disorders. 29587413 2018
CUI: C0009782
Disease: Connective Tissue Diseases
Connective Tissue Diseases 		0.020 Biomarker group BEFREE These data suggest that fibronectin receptor is closely related to the pathogenesis of hereditary connective tissue diseases. 2144868 1990