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X-linked intellectual disability-psychosis-macroorchidism syndrome

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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.

Synonyms

  • Lindsay-Burn syndrome
  • MRXS13
  • PPM-X
  • PPM-X syndrome
  • X-linked intellectual disability 79
  • X-linked intellectual disability with spasticity
  • X-linked mental retardation 79
  • X-linked mental retardation with spasticity
  • intellectual deficit, X-linked - psychosis - macroorchidism
  • intellectual developmental disorder, X-linked, syndromic 13, X-linked recessive
  • intellectual disability psychosis macroorchidism
  • intellectual disability with psychosis, pyramidal signs, and macroorchidism
  • intellectual disability, X-linked 16
  • intellectual disability, X-linked 79
  • intellectual disability, X-linked, syndromic 13
  • intellectual disability, X-linked, syndromic type 13
  • intellectual disability, X-linked, with spasticity
  • mental retardation psychosis macroorchidism
  • mental retardation with psychosis, pyramidal signs, and macroorchidism
  • mental retardation, X-linked 16
  • mental retardation, X-linked 79
  • mental retardation, X-linked, syndromic 13
  • mental retardation, X-linked, syndromic type 13
  • mental retardation, X-linked, with spasticity
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).

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Orphanet

Orphanet has a summary about this condition that may include information on the diagnosis, care, and treatment as well as other resources. Some of the information and resources are available in languages other than English. The summary may include medical terms, so we encourage you to share and discuss this information with your doctor. Orphanet is the French National Institute for Health and Medical Research and the Health Programme of the European Union.

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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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GeneReviews

GeneReviews has an article on this condition covering diagnosis, management, and inheritance. Each article is written by one or more experts on the specific disease and is reviewed by other specialists. The article contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. The GeneReviews database is managed by the University of Washington.

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