APOA1, apolipoprotein A1, 335

N. diseases: 416; N. variants: 32
Disease: Amyloid Neuropathies, Familial ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
Amyloid Neuropathies, Familial 		0.010 GeneticVariation group BEFREE Familial amyloid polyneuropathy (FAP) is most commonly associated with variant plasma transthyretin, although it has also been described in association with mutant apolipoprotein A-1 and gelsolin. 8293178 1993