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intellectual disability, autosomal recessive 59

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Disease Overview

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the IMPA1 gene.

Synonyms

  • IMPA1 autosomal recessive non-syndromic intellectual disability
  • MRT59
  • autosomal recessive non-syndromic intellectual disability caused by mutation in IMPA1
  • intellectual disability, autosomal recessive 59
  • intellectual disability, autosomal recessive type 59
  • mental retardation, autosomal recessive 59
  • mental retardation, autosomal recessive type 59
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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