FGA, fibrinogen alpha chain, 2243

N. diseases: 118; N. variants: 20
Disease: Primary amyloidosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268381
Disease: Primary amyloidosis
Primary amyloidosis 		0.010 GeneticVariation disease BEFREE The mutation underlying Glu526Val fibrinogen alpha-chain amyloidosis is incompletely penetrant and has a variable phenotype that can clinically mimic AL amyloidosis. 10825402 2000