MBL2, mannose binding lectin 2, 4153

N. diseases: 563; N. variants: 21
Disease: Premature Birth ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0151526
Disease: Premature Birth
Premature Birth 		0.300 Biomarker phenotype CTD_human Our data add to the knowledge about genetic predisposition to prematurity and suggest that the fetal MBL2 genotype might be an additional genetic factor contributing to the risk of premature delivery. 16912583 2006