APOA1, apolipoprotein A1, 335

N. diseases: 416; N. variants: 32
Disease: Laryngeal amyloidosis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0339882
Disease: Laryngeal amyloidosis
Laryngeal amyloidosis 		0.010 Biomarker disease BEFREE Laryngeal symptoms may be the presenting feature of hereditary systemic AApoAI amyloidosis, and comprehensive investigations including apoA-I genotyping are warranted in patients who present with apparently localized laryngeal amyloidosis. 19235761 2009