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intellectual disability, X-linked 99, syndromic, female-restricted

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Disease Overview

Any X-linked syndromic intellectual disability in which the cause of the disease is a mutation in the USP9X gene.

Synonyms

  • MRXS99F
  • USP9X X-linked syndromic intellectual disability
  • X-linked syndromic intellectual disability caused by mutation in USP9X
  • intellectual developmental disorder, X-linked 99, syndromic, female-restricted, X-linked dominant
  • intellectual disability, X-linked 99, syndromic, female-restricted
  • mental retardation, X-linked 99, syndromic, female-restricted
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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