SERPIND1, serpin family D member 1, 3053

N. diseases: 60; N. variants: 5
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0162429
Disease: Malnutrition
Malnutrition
0.010 Biomarker disease BEFREE We encountered a congenital HCII deficiency patient with advanced multiple atherosclerotic lesions. 19729870 2009