The association between MORC2 (MORC Family CW-Type Zinc Finger 2) and Developmental Delay, Impaired Growth, Dysmorphic Facies, And Axonal Neuropathy is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and causative variation.
Sources4
Clinical variants54
Symptoms77
Compounds0
Trials0
Publications9
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.