National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Chromosome 7p deletion


Other Names:
Deletion 7p; Monosomy 7p; 7p deletion; Deletion 7p; Monosomy 7p; 7p deletion; 7p monosomy; Partial monosomy 7p See More
Categories:
Chromosome 7p deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the short arm (p) of chromosome 7. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved. Features that often occur in people with chromosome 7p deletion include developmental delay, intellectual disability, behavioral problems, and distinctive facial features. Most cases are not inherited, but people can pass the deletion on to their children. Treatment is based on the signs and symptoms present in each person.[1]
Last updated: 12/1/2015

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Organizations Supporting this Disease

These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.

Where to Start

  • Genetics Home Reference (GHR) contains information on Chromosome 7p deletion. This website is maintained by the National Library of Medicine.
  • The National Organization for Rare Disorders (NORD) has a report for patients and families about this condition. NORD is a patient advocacy organization for individuals with rare diseases and the organizations that serve them.

In-Depth Information

  • PubMed is a searchable database of medical literature and lists journal articles that discuss Chromosome 7p deletion. Click on the link to view a sample search on this topic.

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  1. Chromosome 7, Partial Monosomy 7p. NORD. 2009; http://rarediseases.org/rare-diseases/chromosome-7-partial-monosomy-7p/.