The association between TTI1 (TELO2 Interacting Protein 1) and Neurodevelopmental Disorder With Microcephaly And Movement Abnormalities is well established and manually curated, with its 3 contributing sources — 3 of them expert-curated — recording a known molecular basis, likely-pathogenic variants, and causative variation.
Sources3
Clinical variants8
Symptoms74
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.
