IFNL3, interferon lambda 3, 282617

N. diseases: 175; N. variants: 8
Disease: Hepatic Fibrosis, Congenital ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital 		0.300 Biomarker disease CTD_human IFN-λ3, not IFN-λ4, likely mediates IFNL3-IFNL4 haplotype-dependent hepatic inflammation and fibrosis. 28394349 2017