The association between GOLGA2 (Golgin A2) and Developmental Delay With Hypotonia, Myopathy, And Brain Abnormalities is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.
Sources3
Clinical variants5
Symptoms45
Compounds0
Trials0
Publications3
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.