Additional Resources

Section

Get Information about a Rare Disease

Use the form below to explore NORD's comprehensive rare disease database. Search for detailed information on rare diseases, including NORD's authoritative Rare Disease Reports and data from other reliable sources.
* = NORD Rare Disease Report

Interested in exploring the database in detail?
Click here to explore the database in alphabetical order.

intellectual disability, X-linked, with or without seizures, arx-related

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

Connect & Download

Synonyms

  • ARX-related intellectual disability
  • MRX52
  • MRXARX
  • intellectual developmental disorder, X-linked 29, X-linked recessive
  • intellectual disability, X-linked 29
  • intellectual disability, X-linked 32
  • intellectual disability, X-linked 33
  • intellectual disability, X-linked 38
  • intellectual disability, X-linked 43
  • intellectual disability, X-linked 52
  • intellectual disability, X-linked 54
  • intellectual disability, X-linked 76
  • intellectual disability, X-linked 87
  • intellectual disability, X-linked, with or without seizures, ARX-related
  • intellectual disability, X-linked, with or without seizures, arx-RELATED
  • mental retardation, X-linked 29
  • mental retardation, X-linked 32
  • mental retardation, X-linked 33
  • mental retardation, X-linked 38
  • mental retardation, X-linked 43
  • mental retardation, X-linked 52
  • mental retardation, X-linked 54
  • mental retardation, X-linked 76
  • mental retardation, X-linked 87
  • mental retardation, X-linked, with or without seizures, arx-RELATED
  • mental retardation, X-linked, with or without seizures, arx-related
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

View report
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.

View report
Sign Up for NORD News

Access State Report Card Data

Please complete this form to access the requested resource.

Please consider sharing some basic information with us.

Name(Required)
Consent(Required)
This field is hidden when viewing the form