Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the TBL1XR1 gene. The disease is Monarch Disease Ontology id MONDO_0014842 (intellectual disability, autosomal dominant 41). Also known as: MRD41, TBL1XR1 autosomal dominant non-syndromic intellectual disability, autosomal dominant intellectual disability 41, autosomal dominant mental retardation 41, autosomal dominant non-syndromic intellectual disability caused by mutation in TBL1XR1, intellectual disability, autosomal dominant type 41, mental retardation, autosomal dominant 41, mental retardation, autosomal dominant type 41.