Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the EPB41L1 gene. The disease is MONDO_0013658 (intellectual disability, autosomal dominant 11). Also known as: EPB41L1 autosomal dominant non-syndromic intellectual disability, MRD11, autosomal dominant intellectual disability 11, autosomal dominant mental retardation 11, autosomal dominant non-syndromic intellectual disability caused by mutation in EPB41L1, intellectual developmental disorder, autosomal dominant 11, intellectual disability, autosomal dominant type 11, mental retardation, autosomal dominant type 11.