The association between ATAD3A (ATPase Family AAA Domain Containing 3A) and Cerebellar Hypoplasia/Atrophy, Epilepsy, And Global Developmental Delay is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.
Sources1
Clinical variants1
Symptoms24
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.