has material basis in germline mutation in disease has feature NAA10 Abnormality of the skeletal system Intellectual disability Hypotonia Abnormality of the cardiovascular system Abnormal facial shape Neurodevelopmental delay autism spectrum disorder X-linked syndromic intellectual disability NAA10-related syndrome https://github.com/monarch-initiative/mondo/issues/5588 MONDO:0100124 NAA10-related syndrome NAA10 X-linked syndromic intellectual disability GARD:0026055 X-linked syndromic intellectual disability caused by mutation in NAA10 Ab X-linked syndromic intellectual disability in which the cause of the disease is a mutation in the NAA10 gene. Patients with variants in the NAA10 gene demonstrate symptoms such as developmental delay, intellectual disability, autism spectrum disorder, hypotonia, facial dysmorphism, cardiac anomalies, and/or skeletal anomalies.