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intellectual disability, autosomal dominant 41

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Disease Overview

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the TBL1XR1 gene.

Synonyms

  • MRD41
  • TBL1XR1 autosomal dominant non-syndromic intellectual disability
  • autosomal dominant intellectual disability 41
  • autosomal dominant mental retardation 41
  • autosomal dominant non-syndromic intellectual disability 41
  • autosomal dominant non-syndromic intellectual disability caused by mutation in TBL1XR1
  • intellectual disability, autosomal dominant 41
  • intellectual disability, autosomal dominant type 41
  • mental retardation, autosomal dominant 41
  • mental retardation, autosomal dominant type 41
OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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