The association between FCN3 (Ficolin 3) and Ficolin 3 Deficiency is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording a known molecular basis and likely-pathogenic variants.
Sources2
Clinical variants9
Symptoms9
Compounds0
Trials0
Publications0
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.