The association between SHQ1 (SHQ1, H/ACA Ribonucleoprotein Assembly Factor) and Neurodevelopmental Disorder With Dystonia And Seizures is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.
Sources3
Clinical variants4
Symptoms36
Compounds0
Trials0
Publications2
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.