APOC3, apolipoprotein C3, 345

N. diseases: 153; N. variants: 15
Disease: Hereditary systemic amyloidosis ×
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 D25V apolipoprotein C-III variant causes dominant hereditary systemic amyloidosis and confers cardiovascular protective lipoprotein profile. 26790392 2016