The association between TMEM38B (Transmembrane Protein 38B) and Osteogenesis Imperfecta, Type Xiv is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic and likely-pathogenic variants.
Sources3
Clinical variants12
Symptoms28
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.