SERPINB1, serpin family B member 1, 1992

N. diseases: 41; N. variants: 2
Disease: Cohen syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265223
Disease: Cohen syndrome
Cohen syndrome 		0.010 AlteredExpression disease BEFREE Furthermore, a striking decrease in the expression of SERPINB1 gene, which encodes a critical component of neutrophil survival, was detected in CS neutrophils. 30843084 2019