Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the EEF1A2 gene. The disease is MONDO_0014617 (intellectual disability, autosomal dominant 38). Also known as: EEF1A2 autosomal dominant non-syndromic intellectual disability, MRD38, PRELDS, autosomal dominant intellectual disability 38, autosomal dominant mental retardation 38, autosomal dominant non-syndromic intellectual disability caused by mutation in EEF1A2, intellectual disability, autosomal dominant type 38, mental retardation, autosomal dominant type 38.