The association between PMP22 (Peripheral Myelin Protein 22) and Charcot-Marie-Tooth Disease Type 1a is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.
Sources3
Clinical variants34
Symptoms26
Compounds0
Trials0
Publications24
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.