The association between MCM5 (Minichromosome Maintenance Complex Component 5) and Meier-Gorlin Syndrome 8 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.
Sources4
Clinical variants4
Symptoms19
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.