The association between FBN1 (Fibrillin 1) and Mccune-Albright Syndrome is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic and likely-pathogenic variants.
Sources3
Clinical variants367
Symptoms135
Compounds0
Trials0
Publications11
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.