Intellectual Disability Syndrome Due to a Dyrk1a Point Mutation, is also known as dyrk1a-related intellectual disability syndrome due to a point mutation. An important gene associated with Intellectual Disability Syndrome Due to a Dyrk1a Point Mutation is DYRK1A (Dual Specificity Tyrosine Phosphorylation Regulated Kinase 1A). Affiliated tissues include pituitary and kidney, and related phenotypes are intellectual disability and global developmental delay