LYZ, lysozyme, 4069

N. diseases: 178; N. variants: 8
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 Hereditary lysozyme amyloidosis -- phenotypic heterogeneity and the role of solid organ transplantation. 21988333 2012
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 Biomarker disease GENOMICS_ENGLAND Nonneuropathic amyloidoses (Ostertag type amyloidosis) include those due to abnormalities in lysozyme, fibrinogen Aalpha-chain, and apolipoprotein A-I and A-II. 16523055 2006
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 GeneticVariation disease UNIPROT Human lysozyme gene mutations cause hereditary systemic amyloidosis. 8464497 1993
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 Biomarker disease GENOMICS_ENGLAND Familial nephropathic non-neuropathic amyloidosis: clinical features, immunohistochemistry and chemistry. 1808634 1991
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 Biomarker disease GENOMICS_ENGLAND
CUI: C0268389
Disease: Amyloidosis, familial visceral
Amyloidosis, familial visceral 		0.700 CausalMutation disease CLINVAR