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distal monosomy 10p

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.

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Disease Overview

Distal monosomy 10p is a rare chromosomal disorder in which the tip of the short arm (p arm) of chromosome 10 is deleted resulting in a variable phenotype depending on the size of the deletion. The deletion may involve only the terminal 10p15 band, or extend towards the centromere to bands 10p14 or 10p13.

Synonyms

  • 10p deletion
  • 10p monosomy
  • 10p13-p14 Deletion syndrome
  • Dgs2
  • DiGeorge syndrome type 2
  • DiGeorge syndrome/velocardiofacial syndrome Complex type 2
  • DiGeorge syndrome/velocardiofacial syndrome complex 2
  • DiGeorge syndrome/velocardiofacial syndrome complex-2
  • chromosome 10p deletion
  • deletion 10p
  • distal 10p deletion
  • distal monosomy type 10p
  • monosomy 10p
  • monosomy 10pter
  • partial monosomy 10p
  • telomeric deletion 10p
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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