The association between PLEKHM1 (Pleckstrin Homology And RUN Domain Containing M1) and Osteopetrosis, Autosomal Recessive 6 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.
Sources4
Clinical variants3
Symptoms30
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.