APOA1, apolipoprotein A1, 335

N. diseases: 416; N. variants: 32
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4081731
Disease: Hereditary systemic amyloidosis
Hereditary systemic amyloidosis
0.010 GeneticVariation disease BEFREE The leucine-75-proline variant of apolipoprotein A-I leads to a new hereditary systemic amyloidosis involving mostly the liver and kidney. 18285420 2008