FGA, fibrinogen alpha chain, 2243

N. diseases: 118; N. variants: 20
Disease: Amyloidosis, familial visceral ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 Biomarker disease GENOMICS_ENGLAND Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency. 25427968 2015
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 Biomarker disease GENOMICS_ENGLAND Hereditary amyloidosis caused by R554L fibrinogen Aα-chain mutation in a Spanish family and review of the literature. 23551149 2013
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 GeneticVariation disease UNIPROT Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain. 8097946 1993
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 Biomarker disease GENOMICS_ENGLAND Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain. 8097946 1993
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 Biomarker disease CTD_human
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 CausalMutation disease CLINVAR