The association between OXR1 (Oxidation Resistance 1) and Cerebellar Hypoplasia/Atrophy, Epilepsy, And Global Developmental Delay is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and likely-pathogenic variants.
Sources3
Clinical variants12
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.