The association between FBN1 (Fibrillin 1) and Weill-Marchesani Syndrome 2 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis and pathogenic and likely-pathogenic variants.
Sources4
Clinical variants326
Symptoms81
Compounds0
Trials0
Publications1
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.