The association between LMBR1 (Limb Development Membrane Protein 1) and Polydactyly, Preaxial Ii is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording likely-pathogenic variants and a causative germline mutation.
Sources3
Clinical variants124
Symptoms17
Compounds0
Trials0
Publications12
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.