The association between MPZ (Myelin Protein Zero) and Charcot-Marie-Tooth Disease, Axonal, Type 2i is well established and manually curated, with its 4 contributing sources — 4 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and a causative germline mutation.
Sources4
Clinical variants30
Symptoms16
Compounds0
Trials0
Publications5
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.