Disease: Amyloid nephropathy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268382
Disease: Amyloid nephropathy
Amyloid nephropathy 		0.020 GeneticVariation disease BEFREE Mutations in the fibrinogen A alpha-chain gene are the most common cause of hereditary renal amyloidosis in the United Kingdom. 19073821 2009
CUI: C0268382
Disease: Amyloid nephropathy
Amyloid nephropathy 		0.020 GeneticVariation disease BEFREE A frame shift mutation in the fibrinogen A alpha chain gene in a kindred with renal amyloidosis. 8639778 1996