The association between SIAH1 (Siah E3 Ubiquitin Protein Ligase 1) and Buratti-Harel Syndrome is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.
Sources4
Clinical variants11
Symptoms56
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.