Disease: Amyloidosis, Familial ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0740340
Disease: Amyloidosis, Familial
Amyloidosis, Familial 		0.010 GeneticVariation disease LHGDN Gelsolin domain 2 Ca2+ affinity determines susceptibility to furin proteolysis and familial amyloidosis of finnish type. 14596804 2003