The association between INTS1 (Integrator Complex Subunit 1) and Neurodevelopmental Disorder With Cataracts, Poor Growth, And Dysmorphic Facies 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 variants59
Symptoms68
Compounds0
Trials0
Publications3
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.