has material basis in germline mutation in TBL1XR1 intellectual disability, autosomal dominant 41 https://www.malacards.org/card/intellectual_developmental_disorder_autosomal_dominant_41 OMIM:616944 Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the TBL1XR1 gene. intellectual disability, autosomal dominant type 41 MEDGEN:934751 mental retardation, autosomal dominant 41 GARD:0025023 mental retardation, autosomal dominant type 41 UMLS:C4310784 DOID:0070071 autosomal dominant non-syndromic intellectual disability caused by mutation in TBL1XR1 autosomal dominant intellectual disability 41 intellectual disability, autosomal dominant 41 TBL1XR1 autosomal dominant non-syndromic intellectual disability MONDO:0014842 MRD41 autosomal dominant non-syndromic intellectual disability