Thus, biallelic variants in EMC1 have been linked to the cerebellar atrophy, visual impairment, and psychomotor retardation syndrome (MIM: 616875),4, 5, 6, 7 and hitherto two homozygous loss‐of‐function (LOF) variants in EMC10 have been associated with the neurodevelopmental disorder (NDD) with dysmorphic facies and variable seizures (MIM: 619264) in eight families.8, 9, 10. Here, EMC10 is linked to neurodevelopmental disorder.