The association between GLI1 (GLI Family Zinc Finger 1) and Polydactyly, Preaxial I is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and a causative germline mutation.
Sources3
Clinical variants4
Symptoms5
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.