intellectual disability, X-linked 93

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

Disease Overview

Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the BRWD3 gene.


Synonyms

  • BRWD3 non-syndromic X-linked intellectual disability
  • MRX93
  • intellectual developmental disorder, X-linked 93, X-linked recessive
  • intellectual disability, X-linked 93
  • intellectual disability, X-linked type 93
  • intellectual disability, X-linked, with macrocephaly
  • mental retardation, X-linked 93
  • mental retardation, X-linked type 93
  • mental retardation, X-linked, with macrocephaly
  • non-syndromic X-linked intellectual disability caused by mutation in BRWD3

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

Access State Report Card Data

Please complete this form to access the requested resource.

Please consider sharing some basic information with us.

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