A2M, alpha-2-macroglobulin, 2

N. diseases: 147; N. variants: 3
Disease: AURAL ATRESIA, CONGENITAL ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
AURAL ATRESIA, CONGENITAL 		0.010 GeneticVariation disease BEFREE Our results suggest that the A2M deletion polymorphism may not be a definitive risk factor of CAA in the elderly, although further study with larger samples is necessary to confirm this. 10548657 1999